Canonical Allele Identifier: CA1845635348

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647119A= , CM000671.2:g.34647119A=	GRCh38
NC_000009.11:g.34647116A= , CM000671.1:g.34647116A=	GRCh37
NC_000009.10:g.34637116A=	NCBI36
NG_009029.1:g.5482A=
NG_009029.2:g.5531A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.113A=	ENSP00000509954.1:p.Gln38=
ENST00000378842.8:c.113A= MANE Select	ENSP00000368119.4:p.Gln38=
ENST00000378842.7:c.113A=	ENSP00000368119.3:p.Gln38=
ENST00000450095.6:c.-90A=	ENSP00000401956.2:n.-90A=
ENST00000465543.6:n.452A=
ENST00000468099.2:n.155-2A=
ENST00000472111.5:n.154A=
ENST00000473506.6:c.113A=	ENSP00000432839.2:p.Gln38=
ENST00000473529.5:n.160A=
ENST00000485531.1:n.106A=
ENST00000487381.5:n.139A=
ENST00000489643.6:n.143A=
ENST00000554085.5:c.113A=	ENSP00000450419.1:p.Gln38=
ENST00000554139.5:n.166A=
ENST00000554330.5:n.110A=
ENST00000554550.5:c.113A=	ENSP00000451435.1:p.Gln38=
ENST00000554638.5:n.137A=
ENST00000554897.5:c.113A=	ENSP00000450942.1:p.Gln38=
ENST00000554944.5:n.143A=
ENST00000555020.5:n.143A=
ENST00000555086.5:n.117A=
ENST00000555214.5:n.122A=
ENST00000556157.1:n.220A=
ENST00000556278.1:c.113A=	ENSP00000451792.1:p.Gln38=
ENST00000556403.5:n.126A=
ENST00000556494.5:n.145A=
ENST00000557541.5:n.306A=
ENST00000557706.5:n.227A=
ENST00000605275.1:n.651A=
NM_000155.3:c.113A=	NP_000146.2:p.Gln38=
NM_001258332.1:c.-90A=	NP_001245261.1:n.-90A=
NM_000155.4:c.113A= MANE Select	NP_000146.2:p.Gln38=
NM_001258332.2:c.-90A=	NP_001245261.1:n.-90A=