Canonical Allele Identifier: CA1845640705

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649098A= , CM000671.2:g.34649098A=	GRCh38
NC_000009.11:g.34649095A= , CM000671.1:g.34649095A=	GRCh37
NC_000009.10:g.34639095A=	NCBI36
NG_009029.1:g.7461A=
NG_028966.1:g.1914A=
NG_009029.2:g.7510A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*492+17A=	ENSP00000509954.1:n.*492+17A=
ENST00000378842.8:c.904+17A= MANE Select	ENSP00000368119.4:n.904+17A=
ENST00000378842.7:c.904+17A=	ENSP00000368119.3:n.904+17A=
ENST00000450095.6:c.577+17A=	ENSP00000401956.2:n.577+17A=
ENST00000488412.2:n.177A=
ENST00000489643.6:n.1001A=
ENST00000554550.5:c.*524+17A=	ENSP00000451435.1:n.*524+17A=
ENST00000554638.5:n.1376+17A=
ENST00000555020.5:n.1382A=
ENST00000555086.5:n.1028A=
ENST00000555754.1:n.352+17A=
ENST00000556278.1:c.432+642A=	ENSP00000451792.1:n.432+642A=
ENST00000557706.5:n.1479+17A=
NM_000155.3:c.904+17A=	NP_000146.2:n.904+17A=
NM_001258332.1:c.577+17A=	NP_001245261.1:n.577+17A=
NM_000155.4:c.904+17A= MANE Select	NP_000146.2:n.904+17A=
NM_001258332.2:c.577+17A=	NP_001245261.1:n.577+17A=