Canonical Allele Identifier: CA2649174311

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173910084-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910084A>C , CM000663.2:g.173910084A>C	GRCh38
NC_000001.10:g.173879222A>C , CM000663.1:g.173879222A>C	GRCh37
NC_000001.9:g.172145845A>C	NCBI36
NG_012462.1:g.12295T>G , LRG_577:g.12295T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-142T>G MANE Select	ENSP00000356671.3:n.763-142T>G
ENST00000367698.3:c.763-142T>G	ENSP00000356671.3:n.763-142T>G
ENST00000487183.1:n.414-142T>G
ENST00000617423.4:c.559+1780T>G	ENSP00000478688.1:n.559+1780T>G
NM_000488.3:c.763-142T>G , LRG_577t1:c.763-142T>G	NP_000479.1:n.763-142T>G
XM_005245198.2:c.619-142T>G	XP_005245255.1:n.619-142T>G
NM_001365052.1:c.619-142T>G	NP_001351981.1:n.619-142T>G
NM_000488.4:c.763-142T>G MANE Select	NP_000479.1:n.763-142T>G
NM_001365052.2:c.619-142T>G	NP_001351981.1:n.619-142T>G
NM_001386302.1:c.886-142T>G	NP_001373231.1:n.886-142T>G
NM_001386303.1:c.844-142T>G	NP_001373232.1:n.844-142T>G
NM_001386304.1:c.742-142T>G	NP_001373233.1:n.742-142T>G
NM_001386305.1:c.763-199T>G	NP_001373234.1:n.763-199T>G
NM_001386306.1:c.547-142T>G	NP_001373235.1:n.547-142T>G