Canonical Allele Identifier: CA420603304

Gene: HJV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018578T>C , CM000663.2:g.146018578T>C	GRCh38
NC_000001.10:g.145416435A>G , CM000663.1:g.145416435A>G	GRCh37
NC_000001.9:g.144127792A>G	NCBI36
NG_011568.1:g.8245A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213653.4:c.780A>G MANE Select	NP_998818.1:p.Gly260=
ENST00000336751.11:c.780A>G MANE Select	ENSP00000337014.5:p.Gly260=
NM_001316767.1:c.102A>G	NP_001303696.1:p.Gly34=
NM_001316767.2:c.102A>G	NP_001303696.1:p.Gly34=
NM_001379352.1:c.780A>G	NP_001366281.1:p.Gly260=
NM_145277.4:c.441A>G	NP_660320.3:p.Gly147=
NM_145277.5:c.441A>G	NP_660320.3:p.Gly147=
NM_202004.3:c.102A>G	NP_973733.1:p.Gly34=
NM_202004.4:c.102A>G	NP_973733.1:p.Gly34=
NM_213652.3:c.102A>G	NP_998817.1:p.Gly34=
NM_213652.4:c.102A>G	NP_998817.1:p.Gly34=
NM_213653.3:c.780A>G	NP_998818.1:p.Gly260=
ENST00000336751.10:c.780A>G	ENSP00000337014.5:p.Gly260=
ENST00000357836.5:c.441A>G	ENSP00000350495.5:p.Gly147=
ENST00000475797.1:c.102A>G	ENSP00000425716.1:p.Gly34=
ENST00000497365.5:c.102A>G	ENSP00000421820.1:p.Gly34=
ENST00000634927.1:c.*44A>G	ENSP00000489347.1:n.*44A>G
ENST00000636675.1:c.102A>G	ENSP00000490072.1:p.Gly34=
XM_005272932.1:c.780A>G	XP_005272989.1:p.Gly260=