Canonical Allele Identifier: CA2649174501

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173911674-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911674T>C , CM000663.2:g.173911674T>C	GRCh38
NC_000001.10:g.173880812T>C , CM000663.1:g.173880812T>C	GRCh37
NC_000001.9:g.172147435T>C	NCBI36
NG_012462.1:g.10705A>G , LRG_577:g.10705A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.624+125A>G MANE Select	ENSP00000356671.3:n.624+125A>G
ENST00000367698.3:c.624+125A>G	ENSP00000356671.3:n.624+125A>G
ENST00000487183.1:n.329+125A>G
ENST00000617423.4:c.559+190A>G	ENSP00000478688.1:n.559+190A>G
NM_000488.3:c.624+125A>G , LRG_577t1:c.624+125A>G	NP_000479.1:n.624+125A>G
XM_005245198.2:c.480+125A>G	XP_005245255.1:n.480+125A>G
NM_001365052.1:c.480+125A>G	NP_001351981.1:n.480+125A>G
NM_000488.4:c.624+125A>G MANE Select	NP_000479.1:n.624+125A>G
NM_001365052.2:c.480+125A>G	NP_001351981.1:n.480+125A>G
NM_001386302.1:c.624+125A>G	NP_001373231.1:n.624+125A>G
NM_001386303.1:c.705+125A>G	NP_001373232.1:n.705+125A>G
NM_001386304.1:c.624+125A>G	NP_001373233.1:n.624+125A>G
NM_001386305.1:c.624+125A>G	NP_001373234.1:n.624+125A>G
NM_001386306.1:c.409-783A>G	NP_001373235.1:n.409-783A>G