Canonical Allele Identifier: CA1845639961

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648871A= , CM000671.2:g.34648871A=	GRCh38
NC_000009.11:g.34648868A= , CM000671.1:g.34648868A=	GRCh37
NC_000009.10:g.34638868A=	NCBI36
NG_009029.1:g.7234A=
NG_028966.1:g.1687A=
NG_009029.2:g.7283A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*385A=	ENSP00000509954.1:n.*385A=
ENST00000378842.8:c.797A= MANE Select	ENSP00000368119.4:p.Glu266=
ENST00000378842.7:c.797A=	ENSP00000368119.3:p.Glu266=
ENST00000450095.6:c.470A=	ENSP00000401956.2:p.Glu157=
ENST00000473506.6:c.*385A=	ENSP00000432839.2:n.*385A=
ENST00000489643.6:n.877A=
ENST00000554085.5:c.*541A=	ENSP00000450419.1:n.*541A=
ENST00000554550.5:c.*417A=	ENSP00000451435.1:n.*417A=
ENST00000554638.5:n.1269A=
ENST00000555020.5:n.1258A=
ENST00000555086.5:n.801A=
ENST00000555754.1:n.142A=
ENST00000556244.1:c.784A=
ENST00000556278.1:c.432+415A=	ENSP00000451792.1:n.432+415A=
ENST00000557706.5:n.1359A=
NM_000155.3:c.797A=	NP_000146.2:p.Glu266=
NM_001258332.1:c.470A=	NP_001245261.1:p.Glu157=
NM_000155.4:c.797A= MANE Select	NP_000146.2:p.Glu266=
NM_001258332.2:c.470A=	NP_001245261.1:p.Glu157=