Canonical Allele Identifier: CA1198821000

Gene: HJV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018528T= , CM000663.2:g.146018528T=	GRCh38
NC_000001.10:g.145416485A= , CM000663.1:g.145416485A=	GRCh37
NC_000001.9:g.144127842A=	NCBI36
NG_011568.1:g.8295A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336751.11:c.830A= MANE Select	ENSP00000337014.5:p.Gln277=
ENST00000636675.1:c.152A=	ENSP00000490072.1:p.Gln51=
ENST00000336751.10:c.830A=	ENSP00000337014.5:p.Gln277=
ENST00000357836.5:c.491A=	ENSP00000350495.5:p.Gln164=
ENST00000475797.1:c.152A=	ENSP00000425716.1:p.Gln51=
ENST00000497365.5:c.152A=	ENSP00000421820.1:p.Gln51=
NM_001316767.1:c.152A=	NP_001303696.1:p.Gln51=
NM_145277.4:c.491A=	NP_660320.3:p.Gln164=
NM_202004.3:c.152A=	NP_973733.1:p.Gln51=
NM_213652.3:c.152A=	NP_998817.1:p.Gln51=
NM_213653.3:c.830A=	NP_998818.1:p.Gln277=
XM_005272932.1:c.830A=	XP_005272989.1:p.Gln277=
NM_001316767.2:c.152A=	NP_001303696.1:p.Gln51=
NM_145277.5:c.491A=	NP_660320.3:p.Gln164=
NM_202004.4:c.152A=	NP_973733.1:p.Gln51=
NM_213652.4:c.152A=	NP_998817.1:p.Gln51=
NM_001379352.1:c.830A=	NP_001366281.1:p.Gln277=
NM_213653.4:c.830A= MANE Select	NP_998818.1:p.Gln277=