Canonical Allele Identifier: CA1845638773

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648383C= , CM000671.2:g.34648383C=	GRCh38
NC_000009.11:g.34648380C= , CM000671.1:g.34648380C=	GRCh37
NC_000009.10:g.34638380C=	NCBI36
NG_009029.1:g.6746C=
NG_028966.1:g.1199C=
NG_009029.2:g.6795C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*202C=	ENSP00000509954.1:n.*202C=
ENST00000378842.8:c.614C= MANE Select	ENSP00000368119.4:p.Ser205=
ENST00000378842.7:c.614C=	ENSP00000368119.3:p.Ser205=
ENST00000450095.6:c.287C=	ENSP00000401956.2:p.Ser96=
ENST00000472111.5:n.870C=
ENST00000473506.6:c.*202C=	ENSP00000432839.2:n.*202C=
ENST00000473529.5:n.773C=
ENST00000487381.5:n.999C=
ENST00000489643.6:n.389C=
ENST00000554085.5:c.*358C=	ENSP00000450419.1:n.*358C=
ENST00000554550.5:c.*234C=	ENSP00000451435.1:n.*234C=
ENST00000554638.5:n.1086C=
ENST00000554944.5:n.963C=
ENST00000555020.5:n.770C=
ENST00000555086.5:n.618C=
ENST00000555214.5:n.435C=
ENST00000556244.1:c.601C=
ENST00000556278.1:c.359C=	ENSP00000451792.1:p.Ser120=
ENST00000556494.5:n.735C=
ENST00000557706.5:n.1176C=
NM_000155.3:c.614C=	NP_000146.2:p.Ser205=
NM_001258332.1:c.287C=	NP_001245261.1:p.Ser96=
NM_000155.4:c.614C= MANE Select	NP_000146.2:p.Ser205=
NM_001258332.2:c.287C=	NP_001245261.1:p.Ser96=