Canonical Allele Identifier: CA1207934431
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904153C= , CM000663.2:g.173904153C= GRCh38
NC_000001.10:g.173873291C= , CM000663.1:g.173873291C= GRCh37
NC_000001.9:g.172139914C= NCBI36
NG_012462.1:g.18226G= , LRG_577:g.18226G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-88G= MANE Select ENSP00000356671.3:n.1219-88G=
ENST00000367698.3:c.1219-88G= ENSP00000356671.3:n.1219-88G=
ENST00000617423.4:c.604-88G= ENSP00000478688.1:n.604-88G=
NM_000488.3:c.1219-88G= , LRG_577t1:c.1219-88G= NP_000479.1:n.1219-88G=
XM_005245198.2:c.1075-88G= XP_005245255.1:n.1075-88G=
NM_001365052.1:c.1075-88G= NP_001351981.1:n.1075-88G=
NM_000488.4:c.1219-88G= MANE Select NP_000479.1:n.1219-88G=
NM_001365052.2:c.1075-88G= NP_001351981.1:n.1075-88G=
NM_001386302.1:c.1342-88G= NP_001373231.1:n.1342-88G=
NM_001386303.1:c.1300-88G= NP_001373232.1:n.1300-88G=
NM_001386304.1:c.1198-88G= NP_001373233.1:n.1198-88G=
NM_001386305.1:c.1162-88G= NP_001373234.1:n.1162-88G=
NM_001386306.1:c.1003-88G= NP_001373235.1:n.1003-88G=