Canonical Allele Identifier: CA1207934437
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904188G= , CM000663.2:g.173904188G= GRCh38
NC_000001.10:g.173873326G= , CM000663.1:g.173873326G= GRCh37
NC_000001.9:g.172139949G= NCBI36
NG_012462.1:g.18191C= , LRG_577:g.18191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-123C= MANE Select ENSP00000356671.3:n.1219-123C=
ENST00000367698.3:c.1219-123C= ENSP00000356671.3:n.1219-123C=
ENST00000617423.4:c.604-123C= ENSP00000478688.1:n.604-123C=
NM_000488.3:c.1219-123C= , LRG_577t1:c.1219-123C= NP_000479.1:n.1219-123C=
XM_005245198.2:c.1075-123C= XP_005245255.1:n.1075-123C=
NM_001365052.1:c.1075-123C= NP_001351981.1:n.1075-123C=
NM_000488.4:c.1219-123C= MANE Select NP_000479.1:n.1219-123C=
NM_001365052.2:c.1075-123C= NP_001351981.1:n.1075-123C=
NM_001386302.1:c.1342-123C= NP_001373231.1:n.1342-123C=
NM_001386303.1:c.1300-123C= NP_001373232.1:n.1300-123C=
NM_001386304.1:c.1198-123C= NP_001373233.1:n.1198-123C=
NM_001386305.1:c.1162-123C= NP_001373234.1:n.1162-123C=
NM_001386306.1:c.1003-123C= NP_001373235.1:n.1003-123C=