Canonical Allele Identifier: CA2508759115
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903871G>A , CM000663.2:g.173903871G>A GRCh38
NC_000001.10:g.173873009G>A , CM000663.1:g.173873009G>A GRCh37
NC_000001.9:g.172139632G>A NCBI36
NG_012462.1:g.18508C>T , LRG_577:g.18508C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.*18C>T MANE Select ENSP00000356671.3:n.*18C>T
ENST00000367698.3:c.*18C>T ENSP00000356671.3:n.*18C>T
ENST00000617423.4:c.*18C>T ENSP00000478688.1:n.*18C>T
NM_000488.3:c.*18C>T , LRG_577t1:c.*18C>T NP_000479.1:n.*18C>T
XM_005245198.2:c.*18C>T XP_005245255.1:n.*18C>T
NM_001365052.1:c.*18C>T NP_001351981.1:n.*18C>T
NM_000488.4:c.*18C>T MANE Select NP_000479.1:n.*18C>T
NM_001365052.2:c.*18C>T NP_001351981.1:n.*18C>T
NM_001386302.1:c.*18C>T NP_001373231.1:n.*18C>T
NM_001386303.1:c.*18C>T NP_001373232.1:n.*18C>T
NM_001386304.1:c.*18C>T NP_001373233.1:n.*18C>T
NM_001386305.1:c.*18C>T NP_001373234.1:n.*18C>T
NM_001386306.1:c.*18C>T NP_001373235.1:n.*18C>T