Canonical Allele Identifier: CA1845641060

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649422G= , CM000671.2:g.34649422G=	GRCh38
NC_000009.11:g.34649419G= , CM000671.1:g.34649419G=	GRCh37
NC_000009.10:g.34639419G=	NCBI36
NG_009029.1:g.7785G=
NG_028966.1:g.2238G=
NG_009029.2:g.7834G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*505G=	ENSP00000509954.1:n.*505G=
ENST00000378842.8:c.917G= MANE Select	ENSP00000368119.4:p.Gly306=
ENST00000378842.7:c.917G=	ENSP00000368119.3:p.Gly306=
ENST00000450095.6:c.590G=	ENSP00000401956.2:p.Gly197=
ENST00000488412.2:n.501G=
ENST00000489643.6:n.1325G=
ENST00000554550.5:c.*537G=	ENSP00000451435.1:n.*537G=
ENST00000554638.5:n.1389G=
ENST00000555020.5:n.1706G=
ENST00000555754.1:n.365G=
ENST00000556278.1:c.432+966G=	ENSP00000451792.1:n.432+966G=
ENST00000557706.5:n.1492G=
NM_000155.3:c.917G=	NP_000146.2:p.Gly306=
NM_001258332.1:c.590G=	NP_001245261.1:p.Gly197=
NM_000155.4:c.917G= MANE Select	NP_000146.2:p.Gly306=
NM_001258332.2:c.590G=	NP_001245261.1:p.Gly197=