Canonical Allele Identifier: CA1140886798

Gene: HAX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154275165C= , CM000663.2:g.154275165C=	GRCh38
NC_000001.10:g.154247641C= , CM000663.1:g.154247641C=	GRCh37
NC_000001.9:g.152514265C=	NCBI36
NG_007369.1:g.7603C= , LRG_64:g.7603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435087.2:c.580C=	ENSP00000394920.2:p.Gln194=
ENST00000447768.7:c.504C=	ENSP00000403848.2:p.Pro168=
ENST00000459914.2:n.821C=
ENST00000471326.6:n.1244C=
ENST00000477780.3:n.982C=
ENST00000483970.7:c.592C=	ENSP00000435088.1:p.Gln198=
ENST00000531435.6:n.913C=
ENST00000696929.1:c.*59C=	ENSP00000512978.1:n.*59C=
ENST00000696930.1:n.1241C=
ENST00000696931.1:n.821C=
ENST00000696932.1:c.568C=	ENSP00000512979.1:p.Gln190=
ENST00000696933.1:c.609C=	ENSP00000512980.1:p.Pro203=
ENST00000696938.1:c.559C=	ENSP00000512983.1:p.Gln187=
ENST00000696941.1:c.490C=	ENSP00000512986.1:p.Gln164=
ENST00000696944.1:c.490C=	ENSP00000512989.1:p.Gln164=
ENST00000697592.1:c.490C=	ENSP00000513356.1:p.Gln164=
ENST00000697830.1:c.490C=	ENSP00000513452.1:p.Gln164=
ENST00000328703.12:c.568C= MANE Select	ENSP00000329002.7:p.Gln190=
ENST00000328703.11:c.568C=	ENSP00000329002.7:p.Gln190=
ENST00000435087.1:c.580C=	ENSP00000394920.1:p.Gln194=
ENST00000447768.6:c.504C=	ENSP00000403848.2:p.Pro168=
ENST00000457918.6:c.424C=	ENSP00000411448.2:p.Gln142=
ENST00000459914.1:n.280C=
ENST00000471326.5:n.983C=
ENST00000477780.2:n.982C=
ENST00000483970.6:c.592C=	ENSP00000435088.1:p.Gln198=
ENST00000492550.1:n.157C=
ENST00000531435.5:n.838C=
ENST00000532105.1:c.184C=	ENSP00000433951.1:p.Gln62=
NM_001018837.1:c.424C=	NP_001018238.1:p.Gln142=
NM_006118.3:c.568C= , LRG_64t1:c.568C=	NP_006109.2:p.Gln190=
NM_001018837.2:c.424C=	NP_001018238.1:p.Gln142=
NM_006118.4:c.568C= MANE Select	NP_006109.2:p.Gln190=