Canonical Allele Identifier: CA2649174302

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173910069-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910070del , CM000663.2:g.173910070del	GRCh38
NC_000001.10:g.173879208del , CM000663.1:g.173879208del	GRCh37
NC_000001.9:g.172145831del	NCBI36
NG_012462.1:g.12309del , LRG_577:g.12309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-128del MANE Select	ENSP00000356671.3:n.763-128del
ENST00000367698.3:c.763-128del	ENSP00000356671.3:n.763-128del
ENST00000487183.1:n.414-128del
ENST00000617423.4:c.559+1794del	ENSP00000478688.1:n.559+1794del
NM_000488.3:c.763-128del , LRG_577t1:c.763-128del	NP_000479.1:n.763-128del
XM_005245198.2:c.619-128del	XP_005245255.1:n.619-128del
NM_001365052.1:c.619-128del	NP_001351981.1:n.619-128del
NM_000488.4:c.763-128del MANE Select	NP_000479.1:n.763-128del
NM_001365052.2:c.619-128del	NP_001351981.1:n.619-128del
NM_001386302.1:c.886-128del	NP_001373231.1:n.886-128del
NM_001386303.1:c.844-128del	NP_001373232.1:n.844-128del
NM_001386304.1:c.742-128del	NP_001373233.1:n.742-128del
NM_001386305.1:c.763-185del	NP_001373234.1:n.763-185del
NM_001386306.1:c.547-128del	NP_001373235.1:n.547-128del