Canonical Allele Identifier: CA1845637012

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647848C= , CM000671.2:g.34647848C=	GRCh38
NC_000009.11:g.34647845C= , CM000671.1:g.34647845C=	GRCh37
NC_000009.10:g.34637845C=	NCBI36
NG_009029.1:g.6211C=
NG_028966.1:g.664C=
NG_009029.2:g.6260C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.345C=	ENSP00000509954.1:p.Ser115=
ENST00000378842.8:c.394C= MANE Select	ENSP00000368119.4:p.His132=
ENST00000378842.7:c.394C=	ENSP00000368119.3:p.His132=
ENST00000450095.6:c.67C=	ENSP00000401956.2:p.His23=
ENST00000465543.6:n.733C=
ENST00000472111.5:n.650C=
ENST00000473506.6:c.345C=	ENSP00000432839.2:p.Ser115=
ENST00000473529.5:n.530C=
ENST00000485531.1:n.835C=
ENST00000487381.5:n.779C=
ENST00000489643.6:n.283-267C=
ENST00000554085.5:c.*138C=	ENSP00000450419.1:n.*138C=
ENST00000554139.5:n.573C=
ENST00000554330.5:n.557C=
ENST00000554550.5:c.*14C=	ENSP00000451435.1:n.*14C=
ENST00000554638.5:n.866C=
ENST00000554897.5:c.*14C=	ENSP00000450942.1:n.*14C=
ENST00000554944.5:n.590C=
ENST00000555020.5:n.550C=
ENST00000555086.5:n.398C=
ENST00000555214.5:n.262-200C=
ENST00000556244.1:c.381C=
ENST00000556278.1:c.253-267C=	ENSP00000451792.1:n.253-267C=
ENST00000556494.5:n.515C=
ENST00000557541.5:n.538C=
ENST00000557706.5:n.956C=
NM_000155.3:c.394C=	NP_000146.2:p.His132=
NM_001258332.1:c.67C=	NP_001245261.1:p.His23=
NM_000155.4:c.394C= MANE Select	NP_000146.2:p.His132=
NM_001258332.2:c.67C=	NP_001245261.1:p.His23=