Canonical Allele Identifier: CA1845636421

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647633G= , CM000671.2:g.34647633G=	GRCh38
NC_000009.11:g.34647630G= , CM000671.1:g.34647630G=	GRCh37
NC_000009.10:g.34637630G=	NCBI36
NG_009029.1:g.5996G=
NG_028966.1:g.449G=
NG_009029.2:g.6045G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+66G=	ENSP00000509954.1:n.328+66G=
ENST00000378842.8:c.329-24G= MANE Select	ENSP00000368119.4:n.329-24G=
ENST00000378842.7:c.329-24G=	ENSP00000368119.3:n.329-24G=
ENST00000450095.6:c.51-199G=	ENSP00000401956.2:n.51-199G=
ENST00000465543.6:n.668-24G=
ENST00000472111.5:n.435G=
ENST00000473506.6:c.280-24G=	ENSP00000432839.2:n.280-24G=
ENST00000473529.5:n.441G=
ENST00000485531.1:n.620G=
ENST00000487381.5:n.588-24G=
ENST00000489643.6:n.282+375G=
ENST00000554085.5:c.*73-24G=	ENSP00000450419.1:n.*73-24G=
ENST00000554139.5:n.382-24G=
ENST00000554330.5:n.342G=
ENST00000554550.5:c.253-199G=	ENSP00000451435.1:n.253-199G=
ENST00000554638.5:n.651G=
ENST00000554897.5:c.253-199G=	ENSP00000450942.1:n.253-199G=
ENST00000554944.5:n.375G=
ENST00000555020.5:n.359-24G=
ENST00000555086.5:n.333-24G=
ENST00000555214.5:n.261+375G=
ENST00000556157.1:n.453-24G=
ENST00000556244.1:c.316-24G=
ENST00000556278.1:c.252+375G=	ENSP00000451792.1:n.252+375G=
ENST00000556403.5:n.407G=
ENST00000556494.5:n.426G=
ENST00000557541.5:n.473-24G=
ENST00000557706.5:n.741G=
NM_000155.3:c.329-24G=	NP_000146.2:n.329-24G=
NM_001258332.1:c.51-199G=	NP_001245261.1:n.51-199G=
NM_000155.4:c.329-24G= MANE Select	NP_000146.2:n.329-24G=
NM_001258332.2:c.51-199G=	NP_001245261.1:n.51-199G=