Canonical Allele Identifier: CA2500507293

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173910094-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910094C>A , CM000663.2:g.173910094C>A	GRCh38
NC_000001.10:g.173879232C>A , CM000663.1:g.173879232C>A	GRCh37
NC_000001.9:g.172145855C>A	NCBI36
NG_012462.1:g.12285G>T , LRG_577:g.12285G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-152G>T MANE Select	ENSP00000356671.3:n.763-152G>T
ENST00000367698.3:c.763-152G>T	ENSP00000356671.3:n.763-152G>T
ENST00000487183.1:n.414-152G>T
ENST00000617423.4:c.559+1770G>T	ENSP00000478688.1:n.559+1770G>T
NM_000488.3:c.763-152G>T , LRG_577t1:c.763-152G>T	NP_000479.1:n.763-152G>T
XM_005245198.2:c.619-152G>T	XP_005245255.1:n.619-152G>T
NM_001365052.1:c.619-152G>T	NP_001351981.1:n.619-152G>T
NM_000488.4:c.763-152G>T MANE Select	NP_000479.1:n.763-152G>T
NM_001365052.2:c.619-152G>T	NP_001351981.1:n.619-152G>T
NM_001386302.1:c.886-152G>T	NP_001373231.1:n.886-152G>T
NM_001386303.1:c.844-152G>T	NP_001373232.1:n.844-152G>T
NM_001386304.1:c.742-152G>T	NP_001373233.1:n.742-152G>T
NM_001386305.1:c.763-209G>T	NP_001373234.1:n.763-209G>T
NM_001386306.1:c.547-152G>T	NP_001373235.1:n.547-152G>T