Canonical Allele Identifier: CA1207937084
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910027A= , CM000663.2:g.173910027A= GRCh38
NC_000001.10:g.173879165A= , CM000663.1:g.173879165A= GRCh37
NC_000001.9:g.172145788A= NCBI36
NG_012462.1:g.12352T= , LRG_577:g.12352T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-85T= MANE Select ENSP00000356671.3:n.763-85T=
ENST00000367698.3:c.763-85T= ENSP00000356671.3:n.763-85T=
ENST00000487183.1:n.414-85T=
ENST00000617423.4:c.559+1837T= ENSP00000478688.1:n.559+1837T=
NM_000488.3:c.763-85T= , LRG_577t1:c.763-85T= NP_000479.1:n.763-85T=
XM_005245198.2:c.619-85T= XP_005245255.1:n.619-85T=
NM_001365052.1:c.619-85T= NP_001351981.1:n.619-85T=
NM_000488.4:c.763-85T= MANE Select NP_000479.1:n.763-85T=
NM_001365052.2:c.619-85T= NP_001351981.1:n.619-85T=
NM_001386302.1:c.886-85T= NP_001373231.1:n.886-85T=
NM_001386303.1:c.844-85T= NP_001373232.1:n.844-85T=
NM_001386304.1:c.742-85T= NP_001373233.1:n.742-85T=
NM_001386305.1:c.763-142T= NP_001373234.1:n.763-142T=
NM_001386306.1:c.547-85T= NP_001373235.1:n.547-85T=