Canonical Allele Identifier: CA1207937031
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909874_173909875delinsCT , CM000663.2:g.173909874_173909875delinsCT GRCh38
NC_000001.10:g.173879012_173879013delinsCT , CM000663.1:g.173879012_173879013delinsCT GRCh37
NC_000001.9:g.172145635_172145636delinsCT NCBI36
NG_012462.1:g.12504_12505delinsAG , LRG_577:g.12504_12505delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.830_831delinsAG MANE Select ENSP00000356671.3:p.Glu277=
ENST00000367698.3:c.830_831delinsAG ENSP00000356671.3:p.Glu277=
ENST00000487183.1:n.481_482delinsAG
ENST00000617423.4:c.559+1989_559+1990delinsAG ENSP00000478688.1:n.559+1989_559+1990delinsAG
NM_000488.3:c.830_831delinsAG , LRG_577t1:c.830_831delinsAG NP_000479.1:p.Glu277=
XM_005245198.2:c.686_687delinsAG XP_005245255.1:p.Glu229=
NM_001365052.1:c.686_687delinsAG NP_001351981.1:p.Glu229=
NM_000488.4:c.830_831delinsAG MANE Select NP_000479.1:p.Glu277=
NM_001365052.2:c.686_687delinsAG NP_001351981.1:p.Glu229=
NM_001386302.1:c.953_954delinsAG NP_001373231.1:p.Glu318=
NM_001386303.1:c.911_912delinsAG NP_001373232.1:p.Glu304=
NM_001386304.1:c.809_810delinsAG NP_001373233.1:p.Glu270=
NM_001386305.1:c.773_774delinsAG NP_001373234.1:p.Glu258=
NM_001386306.1:c.614_615delinsAG NP_001373235.1:p.Glu205=