Canonical Allele Identifier: CA915940633
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909727dup , CM000663.2:g.173909727dup GRCh38
NC_000001.10:g.173878865dup , CM000663.1:g.173878865dup GRCh37
NC_000001.9:g.172145488dup NCBI36
NG_012462.1:g.12653dup , LRG_577:g.12653dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.979dup MANE Select ENSP00000356671.3:p.Val327GlyfsTer16
ENST00000367698.3:c.979dup ENSP00000356671.3:p.Val327GlyfsTer16
ENST00000617423.4:c.559+2138dup ENSP00000478688.1:n.559+2138dup
NM_000488.3:c.979dup , LRG_577t1:c.979dup NP_000479.1:p.Val327GlyfsTer16
XM_005245198.2:c.835dup XP_005245255.1:p.Val279GlyfsTer16
NM_001365052.1:c.835dup NP_001351981.1:p.Val279GlyfsTer16
NM_000488.4:c.979dup MANE Select NP_000479.1:p.Val327GlyfsTer16
NM_001365052.2:c.835dup NP_001351981.1:p.Val279GlyfsTer16
NM_001386302.1:c.1102dup NP_001373231.1:p.Val368GlyfsTer16
NM_001386303.1:c.1060dup NP_001373232.1:p.Val354GlyfsTer16
NM_001386304.1:c.958dup NP_001373233.1:p.Val320GlyfsTer16
NM_001386305.1:c.922dup NP_001373234.1:p.Val308GlyfsTer16
NM_001386306.1:c.763dup NP_001373235.1:p.Val255GlyfsTer16