Canonical Allele Identifier: CA1845640168

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648945C= , CM000671.2:g.34648945C=	GRCh38
NC_000009.11:g.34648942C= , CM000671.1:g.34648942C=	GRCh37
NC_000009.10:g.34638942C=	NCBI36
NG_009029.1:g.7308C=
NG_028966.1:g.1761C=
NG_009029.2:g.7357C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*408+51C=	ENSP00000509954.1:n.*408+51C=
ENST00000378842.8:c.820+51C= MANE Select	ENSP00000368119.4:n.820+51C=
ENST00000378842.7:c.820+51C=	ENSP00000368119.3:n.820+51C=
ENST00000450095.6:c.493+51C=	ENSP00000401956.2:n.493+51C=
ENST00000488412.2:n.24C=
ENST00000489643.6:n.900+51C=
ENST00000554085.5:c.*564+51C=	ENSP00000450419.1:n.*564+51C=
ENST00000554550.5:c.*440+51C=	ENSP00000451435.1:n.*440+51C=
ENST00000554638.5:n.1292+51C=
ENST00000555020.5:n.1281+51C=
ENST00000555086.5:n.875C=
ENST00000555754.1:n.216C=
ENST00000556278.1:c.432+489C=	ENSP00000451792.1:n.432+489C=
ENST00000557706.5:n.1395+38C=
NM_000155.3:c.820+51C=	NP_000146.2:n.820+51C=
NM_001258332.1:c.493+51C=	NP_001245261.1:n.493+51C=
NM_000155.4:c.820+51C= MANE Select	NP_000146.2:n.820+51C=
NM_001258332.2:c.493+51C=	NP_001245261.1:n.493+51C=