Canonical Allele Identifier: CA1845636800

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647769G= , CM000671.2:g.34647769G=	GRCh38
NC_000009.11:g.34647766G= , CM000671.1:g.34647766G=	GRCh37
NC_000009.10:g.34637766G=	NCBI36
NG_009029.1:g.6132G=
NG_028966.1:g.585G=
NG_009029.2:g.6181G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-63G=	ENSP00000509954.1:n.329-63G=
ENST00000378842.8:c.378-63G= MANE Select	ENSP00000368119.4:n.378-63G=
ENST00000378842.7:c.378-63G=	ENSP00000368119.3:n.378-63G=
ENST00000450095.6:c.51-63G=	ENSP00000401956.2:n.51-63G=
ENST00000465543.6:n.717-63G=
ENST00000472111.5:n.571G=
ENST00000473506.6:c.329-63G=	ENSP00000432839.2:n.329-63G=
ENST00000473529.5:n.514-63G=
ENST00000485531.1:n.756G=
ENST00000487381.5:n.700G=
ENST00000489643.6:n.283-346G=
ENST00000554085.5:c.*122-63G=	ENSP00000450419.1:n.*122-63G=
ENST00000554139.5:n.494G=
ENST00000554330.5:n.478G=
ENST00000554550.5:c.253-63G=	ENSP00000451435.1:n.253-63G=
ENST00000554638.5:n.787G=
ENST00000554897.5:c.253-63G=	ENSP00000450942.1:n.253-63G=
ENST00000554944.5:n.511G=
ENST00000555020.5:n.471G=
ENST00000555086.5:n.382-63G=
ENST00000555214.5:n.262-279G=
ENST00000556244.1:c.365-63G=
ENST00000556278.1:c.253-346G=	ENSP00000451792.1:n.253-346G=
ENST00000556403.5:n.543G=
ENST00000556494.5:n.499-63G=
ENST00000557541.5:n.522-63G=
ENST00000557706.5:n.877G=
NM_000155.3:c.378-63G=	NP_000146.2:n.378-63G=
NM_001258332.1:c.51-63G=	NP_001245261.1:n.51-63G=
NM_000155.4:c.378-63G= MANE Select	NP_000146.2:n.378-63G=
NM_001258332.2:c.51-63G=	NP_001245261.1:n.51-63G=