Canonical Allele Identifier: CA1845635832

Gene: GALT

Linked Data

• dbSNP Id: rs200439493

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647267G>C , CM000671.2:g.34647267G>C	GRCh38
NC_000009.11:g.34647264G>C , CM000671.1:g.34647264G>C	GRCh37
NC_000009.10:g.34637264G>C	NCBI36
NG_009029.1:g.5630G>C
NG_028966.1:g.83G>C
NG_009029.2:g.5679G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.252+9G>C	ENSP00000509954.1:n.252+9G>C
ENST00000378842.8:c.252+9G>C MANE Select	ENSP00000368119.4:n.252+9G>C
ENST00000378842.7:c.252+9G>C	ENSP00000368119.3:n.252+9G>C
ENST00000450095.6:c.50+9G>C	ENSP00000401956.2:n.50+9G>C
ENST00000465543.6:n.591+9G>C
ENST00000468099.2:n.301G>C
ENST00000472111.5:n.293+9G>C
ENST00000473506.6:c.252+9G>C	ENSP00000432839.2:n.252+9G>C
ENST00000473529.5:n.299+9G>C
ENST00000485531.1:n.254G>C
ENST00000487381.5:n.287G>C
ENST00000489643.6:n.282+9G>C
ENST00000554085.5:c.252+9G>C	ENSP00000450419.1:n.252+9G>C
ENST00000554139.5:n.305+9G>C
ENST00000554330.5:n.249+9G>C
ENST00000554550.5:c.252+9G>C	ENSP00000451435.1:n.252+9G>C
ENST00000554638.5:n.285G>C
ENST00000554897.5:c.252+9G>C	ENSP00000450942.1:n.252+9G>C
ENST00000554944.5:n.282+9G>C
ENST00000555020.5:n.282+9G>C
ENST00000555086.5:n.256+9G>C
ENST00000555214.5:n.261+9G>C
ENST00000556157.1:n.359+9G>C
ENST00000556244.1:c.136+9G>C
ENST00000556278.1:c.252+9G>C	ENSP00000451792.1:n.252+9G>C
ENST00000556403.5:n.265+9G>C
ENST00000556494.5:n.284+9G>C
ENST00000557541.5:n.445+9G>C
ENST00000557706.5:n.375G>C
NM_000155.3:c.252+9G>C	NP_000146.2:n.252+9G>C
NM_001258332.1:c.50+9G>C	NP_001245261.1:n.50+9G>C
NM_000155.4:c.252+9G>C MANE Select	NP_000146.2:n.252+9G>C
NM_001258332.2:c.50+9G>C	NP_001245261.1:n.50+9G>C