Canonical Allele Identifier: CA1143974262
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903901A= , CM000663.2:g.173903901A= GRCh38
NC_000001.10:g.173873039A= , CM000663.1:g.173873039A= GRCh37
NC_000001.9:g.172139662A= NCBI36
NG_012462.1:g.18478T= , LRG_577:g.18478T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1383T= MANE Select ENSP00000356671.3:p.Pro461=
ENST00000367698.3:c.1383T= ENSP00000356671.3:p.Pro461=
ENST00000617423.4:c.768T= ENSP00000478688.1:p.Pro256=
NM_000488.3:c.1383T= , LRG_577t1:c.1383T= NP_000479.1:p.Pro461=
XM_005245198.2:c.1239T= XP_005245255.1:p.Pro413=
NM_001365052.1:c.1239T= NP_001351981.1:p.Pro413=
NM_000488.4:c.1383T= MANE Select NP_000479.1:p.Pro461=
NM_001365052.2:c.1239T= NP_001351981.1:p.Pro413=
NM_001386302.1:c.1506T= NP_001373231.1:p.Pro502=
NM_001386303.1:c.1464T= NP_001373232.1:p.Pro488=
NM_001386304.1:c.1362T= NP_001373233.1:p.Pro454=
NM_001386305.1:c.1326T= NP_001373234.1:p.Pro442=
NM_001386306.1:c.1167T= NP_001373235.1:p.Pro389=