Canonical Allele Identifier: CA1845641587

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649521A= , CM000671.2:g.34649521A=	GRCh38
NC_000009.11:g.34649518A= , CM000671.1:g.34649518A=	GRCh37
NC_000009.10:g.34639518A=	NCBI36
NG_009029.1:g.7884A=
NG_028966.1:g.2337A=
NG_009029.2:g.7933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*604A=	ENSP00000509954.1:n.*604A=
ENST00000378842.8:c.1016A= MANE Select	ENSP00000368119.4:p.Tyr339=
ENST00000378842.7:c.1016A=	ENSP00000368119.3:p.Tyr339=
ENST00000450095.6:c.689A=	ENSP00000401956.2:p.Tyr230=
ENST00000488412.2:n.600A=
ENST00000489643.6:n.1424A=
ENST00000554550.5:c.*636A=	ENSP00000451435.1:n.*636A=
ENST00000554638.5:n.1488A=
ENST00000555020.5:n.1805A=
ENST00000555754.1:n.464A=
ENST00000556278.1:c.432+1065A=	ENSP00000451792.1:n.432+1065A=
ENST00000557706.5:n.1591A=
NM_000155.3:c.1016A=	NP_000146.2:p.Tyr339=
NM_001258332.1:c.689A=	NP_001245261.1:p.Tyr230=
NM_000155.4:c.1016A= MANE Select	NP_000146.2:p.Tyr339=
NM_001258332.2:c.689A=	NP_001245261.1:p.Tyr230=