Canonical Allele Identifier: CA373279960

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647534C>A (hg19) ; chr9:g.34647537C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647537C>A , CM000671.2:g.34647537C>A	GRCh38
NC_000009.11:g.34647534C>A , CM000671.1:g.34647534C>A	GRCh37
NC_000009.10:g.34637534C>A	NCBI36
NG_009029.1:g.5900C>A
NG_028966.1:g.353C>A
NG_009029.2:g.5949C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.298C>A	ENSP00000509954.1:p.Pro100Thr
ENST00000378842.8:c.298C>A MANE Select	ENSP00000368119.4:p.Pro100Thr
ENST00000378842.7:c.298C>A	ENSP00000368119.3:p.Pro100Thr
ENST00000450095.6:c.50+279C>A	ENSP00000401956.2:n.50+279C>A
ENST00000465543.6:n.637C>A
ENST00000472111.5:n.339C>A
ENST00000473506.6:c.253-4C>A	ENSP00000432839.2:n.253-4C>A
ENST00000473529.5:n.345C>A
ENST00000485531.1:n.524C>A
ENST00000487381.5:n.557C>A
ENST00000489643.6:n.282+279C>A
ENST00000554085.5:c.*42C>A	ENSP00000450419.1:n.*42C>A
ENST00000554139.5:n.351C>A
ENST00000554330.5:n.250-4C>A
ENST00000554550.5:c.252+279C>A	ENSP00000451435.1:n.252+279C>A
ENST00000554638.5:n.555C>A
ENST00000554897.5:c.252+279C>A	ENSP00000450942.1:n.252+279C>A
ENST00000554944.5:n.283-4C>A
ENST00000555020.5:n.328C>A
ENST00000555086.5:n.302C>A
ENST00000555214.5:n.261+279C>A
ENST00000556157.1:n.422C>A
ENST00000556244.1:c.285C>A
ENST00000556278.1:c.252+279C>A	ENSP00000451792.1:n.252+279C>A
ENST00000556403.5:n.311C>A
ENST00000556494.5:n.330C>A
ENST00000557541.5:n.446-4C>A
ENST00000557706.5:n.645C>A
NM_000155.3:c.298C>A	NP_000146.2:p.Pro100Thr
NM_001258332.1:c.50+279C>A	NP_001245261.1:n.50+279C>A
NM_000155.4:c.298C>A MANE Select	NP_000146.2:p.Pro100Thr
NM_001258332.2:c.50+279C>A	NP_001245261.1:n.50+279C>A