Canonical Allele Identifier: CA1142052934
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909958A= , CM000663.2:g.173909958A= GRCh38
NC_000001.10:g.173879096A= , CM000663.1:g.173879096A= GRCh37
NC_000001.9:g.172145719A= NCBI36
NG_012462.1:g.12421T= , LRG_577:g.12421T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-16T= MANE Select ENSP00000356671.3:n.763-16T=
ENST00000367698.3:c.763-16T= ENSP00000356671.3:n.763-16T=
ENST00000487183.1:n.414-16T=
ENST00000617423.4:c.559+1906T= ENSP00000478688.1:n.559+1906T=
NM_000488.3:c.763-16T= , LRG_577t1:c.763-16T= NP_000479.1:n.763-16T=
XM_005245198.2:c.619-16T= XP_005245255.1:n.619-16T=
NM_001365052.1:c.619-16T= NP_001351981.1:n.619-16T=
NM_000488.4:c.763-16T= MANE Select NP_000479.1:n.763-16T=
NM_001365052.2:c.619-16T= NP_001351981.1:n.619-16T=
NM_001386302.1:c.886-16T= NP_001373231.1:n.886-16T=
NM_001386303.1:c.844-16T= NP_001373232.1:n.844-16T=
NM_001386304.1:c.742-16T= NP_001373233.1:n.742-16T=
NM_001386305.1:c.763-73T= NP_001373234.1:n.763-73T=
NM_001386306.1:c.547-16T= NP_001373235.1:n.547-16T=