Canonical Allele Identifier: CA1845641651

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649543G= , CM000671.2:g.34649543G=	GRCh38
NC_000009.11:g.34649540G= , CM000671.1:g.34649540G=	GRCh37
NC_000009.10:g.34639540G=	NCBI36
NG_009029.1:g.7906G=
NG_028966.1:g.2359G=
NG_009029.2:g.7955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*626G=	ENSP00000509954.1:n.*626G=
ENST00000378842.8:c.1038G= MANE Select	ENSP00000368119.4:p.Gln346=
ENST00000378842.7:c.1038G=	ENSP00000368119.3:p.Gln346=
ENST00000450095.6:c.711G=	ENSP00000401956.2:p.Gln237=
ENST00000488412.2:n.622G=
ENST00000489643.6:n.1446G=
ENST00000554550.5:c.*658G=	ENSP00000451435.1:n.*658G=
ENST00000554638.5:n.1510G=
ENST00000555020.5:n.1827G=
ENST00000555754.1:n.486G=
ENST00000556278.1:c.432+1087G=	ENSP00000451792.1:n.432+1087G=
ENST00000557706.5:n.1613G=
NM_000155.3:c.1038G=	NP_000146.2:p.Gln346=
NM_001258332.1:c.711G=	NP_001245261.1:p.Gln237=
NM_000155.4:c.1038G= MANE Select	NP_000146.2:p.Gln346=
NM_001258332.2:c.711G=	NP_001245261.1:p.Gln237=