Canonical Allele Identifier: CA2649174487

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173911656-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911656A>T , CM000663.2:g.173911656A>T	GRCh38
NC_000001.10:g.173880794A>T , CM000663.1:g.173880794A>T	GRCh37
NC_000001.9:g.172147417A>T	NCBI36
NG_012462.1:g.10723T>A , LRG_577:g.10723T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.624+143T>A MANE Select	ENSP00000356671.3:n.624+143T>A
ENST00000367698.3:c.624+143T>A	ENSP00000356671.3:n.624+143T>A
ENST00000487183.1:n.329+143T>A
ENST00000617423.4:c.559+208T>A	ENSP00000478688.1:n.559+208T>A
NM_000488.3:c.624+143T>A , LRG_577t1:c.624+143T>A	NP_000479.1:n.624+143T>A
XM_005245198.2:c.480+143T>A	XP_005245255.1:n.480+143T>A
NM_001365052.1:c.480+143T>A	NP_001351981.1:n.480+143T>A
NM_000488.4:c.624+143T>A MANE Select	NP_000479.1:n.624+143T>A
NM_001365052.2:c.480+143T>A	NP_001351981.1:n.480+143T>A
NM_001386302.1:c.624+143T>A	NP_001373231.1:n.624+143T>A
NM_001386303.1:c.705+143T>A	NP_001373232.1:n.705+143T>A
NM_001386304.1:c.624+143T>A	NP_001373233.1:n.624+143T>A
NM_001386305.1:c.624+143T>A	NP_001373234.1:n.624+143T>A
NM_001386306.1:c.409-765T>A	NP_001373235.1:n.409-765T>A