Canonical Allele Identifier: CA1845635643

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647197C= , CM000671.2:g.34647197C=	GRCh38
NC_000009.11:g.34647194C= , CM000671.1:g.34647194C=	GRCh37
NC_000009.10:g.34637194C=	NCBI36
NG_009029.1:g.5560C=
NG_028966.1:g.13C=
NG_009029.2:g.5609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.191C=	ENSP00000509954.1:p.Thr64=
ENST00000378842.8:c.191C= MANE Select	ENSP00000368119.4:p.Thr64=
ENST00000378842.7:c.191C=	ENSP00000368119.3:p.Thr64=
ENST00000450095.6:c.-12C=	ENSP00000401956.2:n.-12C=
ENST00000465543.6:n.530C=
ENST00000468099.2:n.231C=
ENST00000472111.5:n.232C=
ENST00000473506.6:c.191C=	ENSP00000432839.2:p.Thr64=
ENST00000473529.5:n.238C=
ENST00000485531.1:n.184C=
ENST00000487381.5:n.217C=
ENST00000489643.6:n.221C=
ENST00000554085.5:c.191C=	ENSP00000450419.1:p.Thr64=
ENST00000554139.5:n.244C=
ENST00000554330.5:n.188C=
ENST00000554550.5:c.191C=	ENSP00000451435.1:p.Thr64=
ENST00000554638.5:n.215C=
ENST00000554897.5:c.191C=	ENSP00000450942.1:p.Thr64=
ENST00000554944.5:n.221C=
ENST00000555020.5:n.221C=
ENST00000555086.5:n.195C=
ENST00000555214.5:n.200C=
ENST00000556157.1:n.298C=
ENST00000556244.1:c.75C=
ENST00000556278.1:c.191C=	ENSP00000451792.1:p.Thr64=
ENST00000556403.5:n.204C=
ENST00000556494.5:n.223C=
ENST00000557541.5:n.384C=
ENST00000557706.5:n.305C=
NM_000155.3:c.191C=	NP_000146.2:p.Thr64=
NM_001258332.1:c.-12C=	NP_001245261.1:n.-12C=
NM_000155.4:c.191C= MANE Select	NP_000146.2:p.Thr64=
NM_001258332.2:c.-12C=	NP_001245261.1:n.-12C=