Canonical Allele Identifier: CA1845635038

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646864G= , CM000671.2:g.34646864G=	GRCh38
NC_000009.11:g.34646861G= , CM000671.1:g.34646861G=	GRCh37
NC_000009.10:g.34636861G=	NCBI36
NG_009029.1:g.5227G=
NG_009029.2:g.5276G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.82+78G=	ENSP00000509954.1:n.82+78G=
ENST00000378842.8:c.82+78G= MANE Select	ENSP00000368119.4:n.82+78G=
ENST00000378842.7:c.82+78G=	ENSP00000368119.3:n.82+78G=
ENST00000450095.6:c.-121+78G=	ENSP00000401956.2:n.-121+78G=
ENST00000465543.6:n.197G=
ENST00000468099.2:n.154+78G=
ENST00000472111.5:n.123+78G=
ENST00000473506.6:c.82+78G=	ENSP00000432839.2:n.82+78G=
ENST00000473529.5:n.129+78G=
ENST00000485531.1:n.20G=
ENST00000487381.5:n.108+78G=
ENST00000489643.6:n.112+78G=
ENST00000554085.5:c.82+78G=	ENSP00000450419.1:n.82+78G=
ENST00000554139.5:n.135+78G=
ENST00000554330.5:n.76G=
ENST00000554550.5:c.82+78G=	ENSP00000451435.1:n.82+78G=
ENST00000554638.5:n.106+78G=
ENST00000554897.5:c.82+78G=	ENSP00000450942.1:n.82+78G=
ENST00000554944.5:n.112+78G=
ENST00000555020.5:n.112+78G=
ENST00000555086.5:n.83G=
ENST00000555214.5:n.91+78G=
ENST00000556278.1:c.82+78G=	ENSP00000451792.1:n.82+78G=
ENST00000556403.5:n.92G=
ENST00000556494.5:n.59G=
ENST00000557541.5:n.220G=
ENST00000605275.1:n.396G=
NM_000155.3:c.82+78G=	NP_000146.2:n.82+78G=
NM_001258332.1:c.-121+78G=	NP_001245261.1:n.-121+78G=
NM_000155.4:c.82+78G= MANE Select	NP_000146.2:n.82+78G=
NM_001258332.2:c.-121+78G=	NP_001245261.1:n.-121+78G=