Canonical Allele Identifier: CA342132743

Gene: HJV

Linked Data

• gnomAD v4: 1-146018237-G-A
• MyVariant Identifiers: chr1:g.145416776C>T (hg19) ; chr1:g.146018237G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018237G>A , CM000663.2:g.146018237G>A	GRCh38
NC_000001.10:g.145416776C>T , CM000663.1:g.145416776C>T	GRCh37
NC_000001.9:g.144128133C>T	NCBI36
NG_011568.1:g.8586C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.1121C>T MANE Select	ENSP00000337014.5:p.Thr374Ile
ENST00000636675.1:c.443C>T	ENSP00000490072.1:p.Thr148Ile
ENST00000336751.10:c.1121C>T	ENSP00000337014.5:p.Thr374Ile
ENST00000357836.5:c.782C>T	ENSP00000350495.5:p.Thr261Ile
ENST00000475797.1:c.443C>T	ENSP00000425716.1:p.Thr148Ile
ENST00000497365.5:c.443C>T	ENSP00000421820.1:p.Thr148Ile
NM_001316767.1:c.443C>T	NP_001303696.1:p.Thr148Ile
NM_145277.4:c.782C>T	NP_660320.3:p.Thr261Ile
NM_202004.3:c.443C>T	NP_973733.1:p.Thr148Ile
NM_213652.3:c.443C>T	NP_998817.1:p.Thr148Ile
NM_213653.3:c.1121C>T	NP_998818.1:p.Thr374Ile
XM_005272932.1:c.1121C>T	XP_005272989.1:p.Thr374Ile
NM_001316767.2:c.443C>T	NP_001303696.1:p.Thr148Ile
NM_145277.5:c.782C>T	NP_660320.3:p.Thr261Ile
NM_202004.4:c.443C>T	NP_973733.1:p.Thr148Ile
NM_213652.4:c.443C>T	NP_998817.1:p.Thr148Ile
NM_001379352.1:c.1121C>T	NP_001366281.1:p.Thr374Ile
NM_213653.4:c.1121C>T MANE Select	NP_998818.1:p.Thr374Ile