Canonical Allele Identifier: CA1140886752

Gene: HJV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019530A= , CM000663.2:g.146019530A=	GRCh38
NC_000001.10:g.145415483T= , CM000663.1:g.145415483T=	GRCh37
NC_000001.9:g.144126840T=	NCBI36
NG_011568.1:g.7293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.302T= MANE Select	ENSP00000337014.5:p.Leu101=
ENST00000636675.1:c.-22+168T=	ENSP00000490072.1:n.-22+168T=
ENST00000336751.10:c.302T=	ENSP00000337014.5:p.Leu101=
ENST00000357836.5:c.-38T=	ENSP00000350495.5:n.-38T=
ENST00000475797.1:c.-21-830T=	ENSP00000425716.1:n.-21-830T=
ENST00000497365.5:c.-22+168T=	ENSP00000421820.1:n.-22+168T=
ENST00000634927.1:c.134+168T=	ENSP00000489347.1:n.134+168T=
NM_001316767.1:c.-22+168T=	NP_001303696.1:n.-22+168T=
NM_145277.4:c.-38T=	NP_660320.3:n.-38T=
NM_202004.3:c.-22+168T=	NP_973733.1:n.-22+168T=
NM_213652.3:c.-21-830T=	NP_998817.1:n.-21-830T=
NM_213653.3:c.302T=	NP_998818.1:p.Leu101=
XM_005272932.1:c.302T=	XP_005272989.1:p.Leu101=
NM_001316767.2:c.-22+168T=	NP_001303696.1:n.-22+168T=
NM_145277.5:c.-38T=	NP_660320.3:n.-38T=
NM_202004.4:c.-22+168T=	NP_973733.1:n.-22+168T=
NM_213652.4:c.-21-830T=	NP_998817.1:n.-21-830T=
NM_001379352.1:c.302T=	NP_001366281.1:p.Leu101=
NM_213653.4:c.302T= MANE Select	NP_998818.1:p.Leu101=