Canonical Allele Identifier: CA373278266

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34646737G>C (hg19) ; chr9:g.34646740G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646740G>C , CM000671.2:g.34646740G>C	GRCh38
NC_000009.11:g.34646737G>C , CM000671.1:g.34646737G>C	GRCh37
NC_000009.10:g.34636737G>C	NCBI36
NG_009029.1:g.5103G>C
NG_009029.2:g.5152G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.36G>C	ENSP00000509954.1:p.Gln12His
ENST00000378842.8:c.36G>C MANE Select	ENSP00000368119.4:p.Gln12His
ENST00000378842.7:c.36G>C	ENSP00000368119.3:p.Gln12His
ENST00000450095.6:c.-167G>C	ENSP00000401956.2:n.-167G>C
ENST00000465543.6:n.73G>C
ENST00000468099.2:n.108G>C
ENST00000472111.5:n.77G>C
ENST00000473506.6:c.36G>C	ENSP00000432839.2:p.Gln12His
ENST00000473529.5:n.83G>C
ENST00000487381.5:n.62G>C
ENST00000489643.6:n.66G>C
ENST00000554085.5:c.36G>C	ENSP00000450419.1:p.Gln12His
ENST00000554139.5:n.89G>C
ENST00000554550.5:c.36G>C	ENSP00000451435.1:p.Gln12His
ENST00000554638.5:n.60G>C
ENST00000554897.5:c.36G>C	ENSP00000450942.1:p.Gln12His
ENST00000554944.5:n.66G>C
ENST00000555020.5:n.66G>C
ENST00000555214.5:n.45G>C
ENST00000556278.1:c.36G>C	ENSP00000451792.1:p.Gln12His
ENST00000557541.5:n.96G>C
ENST00000605275.1:n.272G>C
NM_000155.3:c.36G>C	NP_000146.2:p.Gln12His
NM_001258332.1:c.-167G>C	NP_001245261.1:n.-167G>C
NM_000155.4:c.36G>C MANE Select	NP_000146.2:p.Gln12His
NM_001258332.2:c.-167G>C	NP_001245261.1:n.-167G>C