Canonical Allele Identifier: CA2649174304

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173910070-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910075del , CM000663.2:g.173910075del	GRCh38
NC_000001.10:g.173879213del , CM000663.1:g.173879213del	GRCh37
NC_000001.9:g.172145836del	NCBI36
NG_012462.1:g.12308del , LRG_577:g.12308del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-129del MANE Select	ENSP00000356671.3:n.763-129del
ENST00000367698.3:c.763-129del	ENSP00000356671.3:n.763-129del
ENST00000487183.1:n.414-129del
ENST00000617423.4:c.559+1793del	ENSP00000478688.1:n.559+1793del
NM_000488.3:c.763-129del , LRG_577t1:c.763-129del	NP_000479.1:n.763-129del
XM_005245198.2:c.619-129del	XP_005245255.1:n.619-129del
NM_001365052.1:c.619-129del	NP_001351981.1:n.619-129del
NM_000488.4:c.763-129del MANE Select	NP_000479.1:n.763-129del
NM_001365052.2:c.619-129del	NP_001351981.1:n.619-129del
NM_001386302.1:c.886-129del	NP_001373231.1:n.886-129del
NM_001386303.1:c.844-129del	NP_001373232.1:n.844-129del
NM_001386304.1:c.742-129del	NP_001373233.1:n.742-129del
NM_001386305.1:c.763-186del	NP_001373234.1:n.763-186del
NM_001386306.1:c.547-129del	NP_001373235.1:n.547-129del