Canonical Allele Identifier: CA1198821490

Gene: HJV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019702C= , CM000663.2:g.146019702C=	GRCh38
NC_000001.10:g.145415311G= , CM000663.1:g.145415311G=	GRCh37
NC_000001.9:g.144126668G=	NCBI36
NG_011568.1:g.7121G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.130G= MANE Select	ENSP00000337014.5:p.Ala44=
ENST00000636675.1:c.-26G=	ENSP00000490072.1:n.-26G=
ENST00000336751.10:c.130G=	ENSP00000337014.5:p.Ala44=
ENST00000357836.5:c.-210G=	ENSP00000350495.5:n.-210G=
ENST00000421822.2:c.130G=	ENSP00000411863.2:p.Ala44=
ENST00000475797.1:c.-21-1002G=	ENSP00000425716.1:n.-21-1002G=
ENST00000497365.5:c.-26G=	ENSP00000421820.1:n.-26G=
ENST00000634927.1:c.130G=	ENSP00000489347.1:p.Ala44=
NM_001316767.1:c.-26G=	NP_001303696.1:n.-26G=
NM_145277.4:c.-210G=	NP_660320.3:n.-210G=
NM_202004.3:c.-26G=	NP_973733.1:n.-26G=
NM_213652.3:c.-21-1002G=	NP_998817.1:n.-21-1002G=
NM_213653.3:c.130G=	NP_998818.1:p.Ala44=
XM_005272932.1:c.130G=	XP_005272989.1:p.Ala44=
NM_001316767.2:c.-26G=	NP_001303696.1:n.-26G=
NM_145277.5:c.-210G=	NP_660320.3:n.-210G=
NM_202004.4:c.-26G=	NP_973733.1:n.-26G=
NM_213652.4:c.-21-1002G=	NP_998817.1:n.-21-1002G=
NM_001379352.1:c.130G=	NP_001366281.1:p.Ala44=
NM_213653.4:c.130G= MANE Select	NP_998818.1:p.Ala44=