Canonical Allele Identifier: CA464596014

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647955G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647958G>T , CM000671.2:g.34647958G>T	GRCh38
NC_000009.11:g.34647955G>T , CM000671.1:g.34647955G>T	GRCh37
NC_000009.10:g.34637955G>T	NCBI36
NG_009029.1:g.6321G>T
NG_028966.1:g.774G>T
NG_009029.2:g.6370G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*92G>T	ENSP00000509954.1:n.*92G>T
ENST00000378842.8:c.504G>T MANE Select	ENSP00000368119.4:p.Val168=
ENST00000378842.7:c.504G>T	ENSP00000368119.3:p.Val168=
ENST00000450095.6:c.177G>T	ENSP00000401956.2:p.Val59=
ENST00000465543.6:n.843G>T
ENST00000472111.5:n.760G>T
ENST00000473506.6:c.*92G>T	ENSP00000432839.2:n.*92G>T
ENST00000473529.5:n.640G>T
ENST00000485531.1:n.945G>T
ENST00000487381.5:n.889G>T
ENST00000489643.6:n.283-157G>T
ENST00000554085.5:c.*248G>T	ENSP00000450419.1:n.*248G>T
ENST00000554139.5:n.683G>T
ENST00000554550.5:c.*124G>T	ENSP00000451435.1:n.*124G>T
ENST00000554638.5:n.976G>T
ENST00000554897.5:c.*124G>T	ENSP00000450942.1:n.*124G>T
ENST00000554944.5:n.700G>T
ENST00000555020.5:n.660G>T
ENST00000555086.5:n.508G>T
ENST00000555214.5:n.262-90G>T
ENST00000556244.1:c.491G>T
ENST00000556278.1:c.253-157G>T	ENSP00000451792.1:n.253-157G>T
ENST00000556494.5:n.625G>T
ENST00000557706.5:n.1066G>T
NM_000155.3:c.504G>T	NP_000146.2:p.Val168=
NM_001258332.1:c.177G>T	NP_001245261.1:p.Val59=
NM_000155.4:c.504G>T MANE Select	NP_000146.2:p.Val168=
NM_001258332.2:c.177G>T	NP_001245261.1:p.Val59=