Canonical Allele Identifier: CA2579753954
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914725_173914728dup , CM000663.2:g.173914725_173914728dup GRCh38
NC_000001.10:g.173883863_173883866dup , CM000663.1:g.173883863_173883866dup GRCh37
NC_000001.9:g.172150486_172150489dup NCBI36
NG_012462.1:g.7651_7654dup , LRG_577:g.7651_7654dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.233_236dup MANE Select ENSP00000356671.3:p.Val80AlafsTer26
ENST00000367698.3:c.233_236dup ENSP00000356671.3:p.Val80AlafsTer26
ENST00000494024.1:n.459_462dup
ENST00000617423.4:c.233_236dup ENSP00000478688.1:p.Val80AlafsTer26
NM_000488.3:c.233_236dup , LRG_577t1:c.233_236dup NP_000479.1:p.Val80AlafsTer26
XM_005245198.2:c.89_92dup XP_005245255.1:p.Val32AlafsTer26
NM_001365052.1:c.89_92dup NP_001351981.1:p.Val32AlafsTer26
NM_000488.4:c.233_236dup MANE Select NP_000479.1:p.Val80AlafsTer26
NM_001365052.2:c.89_92dup NP_001351981.1:p.Val32AlafsTer26
NM_001386302.1:c.233_236dup NP_001373231.1:p.Val80AlafsTer26
NM_001386303.1:c.314_317dup NP_001373232.1:p.Val107AlafsTer26
NM_001386304.1:c.233_236dup NP_001373233.1:p.Val80AlafsTer26
NM_001386305.1:c.233_236dup NP_001373234.1:p.Val80AlafsTer26
NM_001386306.1:c.233_236dup NP_001373235.1:p.Val80AlafsTer26