Canonical Allele Identifier: CA373279086

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647496C>A (hg19) ; chr9:g.34647499C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647499C>A , CM000671.2:g.34647499C>A	GRCh38
NC_000009.11:g.34647496C>A , CM000671.1:g.34647496C>A	GRCh37
NC_000009.10:g.34637496C>A	NCBI36
NG_009029.1:g.5862C>A
NG_028966.1:g.315C>A
NG_009029.2:g.5911C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.260C>A	ENSP00000509954.1:p.Pro87His
ENST00000378842.8:c.260C>A MANE Select	ENSP00000368119.4:p.Pro87His
ENST00000378842.7:c.260C>A	ENSP00000368119.3:p.Pro87His
ENST00000450095.6:c.50+241C>A	ENSP00000401956.2:n.50+241C>A
ENST00000465543.6:n.599C>A
ENST00000468099.2:n.533C>A
ENST00000472111.5:n.301C>A
ENST00000473506.6:c.253-42C>A	ENSP00000432839.2:n.253-42C>A
ENST00000473529.5:n.307C>A
ENST00000485531.1:n.486C>A
ENST00000487381.5:n.519C>A
ENST00000489643.6:n.282+241C>A
ENST00000554085.5:c.*4C>A	ENSP00000450419.1:n.*4C>A
ENST00000554139.5:n.313C>A
ENST00000554330.5:n.250-42C>A
ENST00000554550.5:c.252+241C>A	ENSP00000451435.1:n.252+241C>A
ENST00000554638.5:n.517C>A
ENST00000554897.5:c.252+241C>A	ENSP00000450942.1:n.252+241C>A
ENST00000554944.5:n.283-42C>A
ENST00000555020.5:n.290C>A
ENST00000555086.5:n.264C>A
ENST00000555214.5:n.261+241C>A
ENST00000556157.1:n.384C>A
ENST00000556244.1:c.247C>A
ENST00000556278.1:c.252+241C>A	ENSP00000451792.1:n.252+241C>A
ENST00000556403.5:n.273C>A
ENST00000556494.5:n.292C>A
ENST00000557541.5:n.446-42C>A
ENST00000557706.5:n.607C>A
NM_000155.3:c.260C>A	NP_000146.2:p.Pro87His
NM_001258332.1:c.50+241C>A	NP_001245261.1:n.50+241C>A
NM_000155.4:c.260C>A MANE Select	NP_000146.2:p.Pro87His
NM_001258332.2:c.50+241C>A	NP_001245261.1:n.50+241C>A