Canonical Allele Identifier: CA1845635373

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647130G= , CM000671.2:g.34647130G=	GRCh38
NC_000009.11:g.34647127G= , CM000671.1:g.34647127G=	GRCh37
NC_000009.10:g.34637127G=	NCBI36
NG_009029.1:g.5493G=
NG_009029.2:g.5542G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.124G=	ENSP00000509954.1:p.Val42=
ENST00000378842.8:c.124G= MANE Select	ENSP00000368119.4:p.Val42=
ENST00000378842.7:c.124G=	ENSP00000368119.3:p.Val42=
ENST00000450095.6:c.-79G=	ENSP00000401956.2:n.-79G=
ENST00000465543.6:n.463G=
ENST00000468099.2:n.164G=
ENST00000472111.5:n.165G=
ENST00000473506.6:c.124G=	ENSP00000432839.2:p.Val42=
ENST00000473529.5:n.171G=
ENST00000485531.1:n.117G=
ENST00000487381.5:n.150G=
ENST00000489643.6:n.154G=
ENST00000554085.5:c.124G=	ENSP00000450419.1:p.Val42=
ENST00000554139.5:n.177G=
ENST00000554330.5:n.121G=
ENST00000554550.5:c.124G=	ENSP00000451435.1:p.Val42=
ENST00000554638.5:n.148G=
ENST00000554897.5:c.124G=	ENSP00000450942.1:p.Val42=
ENST00000554944.5:n.154G=
ENST00000555020.5:n.154G=
ENST00000555086.5:n.128G=
ENST00000555214.5:n.133G=
ENST00000556157.1:n.231G=
ENST00000556244.1:c.8G=
ENST00000556278.1:c.124G=	ENSP00000451792.1:p.Val42=
ENST00000556403.5:n.137G=
ENST00000556494.5:n.156G=
ENST00000557541.5:n.317G=
ENST00000557706.5:n.238G=
ENST00000605275.1:n.662G=
NM_000155.3:c.124G=	NP_000146.2:p.Val42=
NM_001258332.1:c.-79G=	NP_001245261.1:n.-79G=
NM_000155.4:c.124G= MANE Select	NP_000146.2:p.Val42=
NM_001258332.2:c.-79G=	NP_001245261.1:n.-79G=