Canonical Allele Identifier: CA2840004210

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648904C>A , CM000671.2:g.34648904C>A	GRCh38
NC_000009.11:g.34648901C>A , CM000671.1:g.34648901C>A	GRCh37
NC_000009.10:g.34638901C>A	NCBI36
NG_009029.1:g.7267C>A
NG_028966.1:g.1720C>A
NG_009029.2:g.7316C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*408+10C>A	ENSP00000509954.1:n.*408+10C>A
ENST00000378842.8:c.820+10C>A MANE Select	ENSP00000368119.4:n.820+10C>A
ENST00000378842.7:c.820+10C>A	ENSP00000368119.3:n.820+10C>A
ENST00000450095.6:c.493+10C>A	ENSP00000401956.2:n.493+10C>A
ENST00000489643.6:n.900+10C>A
ENST00000554085.5:c.*564+10C>A	ENSP00000450419.1:n.*564+10C>A
ENST00000554550.5:c.*440+10C>A	ENSP00000451435.1:n.*440+10C>A
ENST00000554638.5:n.1292+10C>A
ENST00000555020.5:n.1281+10C>A
ENST00000555086.5:n.834C>A
ENST00000555754.1:n.175C>A
ENST00000556278.1:c.432+448C>A	ENSP00000451792.1:n.432+448C>A
ENST00000557706.5:n.1392C>A
NM_000155.3:c.820+10C>A	NP_000146.2:n.820+10C>A
NM_001258332.1:c.493+10C>A	NP_001245261.1:n.493+10C>A
NM_000155.4:c.820+10C>A MANE Select	NP_000146.2:n.820+10C>A
NM_001258332.2:c.493+10C>A	NP_001245261.1:n.493+10C>A