Canonical Allele Identifier: CA464595706

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647539T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647542T>A , CM000671.2:g.34647542T>A	GRCh38
NC_000009.11:g.34647539T>A , CM000671.1:g.34647539T>A	GRCh37
NC_000009.10:g.34637539T>A	NCBI36
NG_009029.1:g.5905T>A
NG_028966.1:g.358T>A
NG_009029.2:g.5954T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.303T>A	ENSP00000509954.1:p.Ala101=
ENST00000378842.8:c.303T>A MANE Select	ENSP00000368119.4:p.Ala101=
ENST00000378842.7:c.303T>A	ENSP00000368119.3:p.Ala101=
ENST00000450095.6:c.50+284T>A	ENSP00000401956.2:n.50+284T>A
ENST00000465543.6:n.642T>A
ENST00000472111.5:n.344T>A
ENST00000473506.6:c.254T>A	ENSP00000432839.2:p.Leu85His
ENST00000473529.5:n.350T>A
ENST00000485531.1:n.529T>A
ENST00000487381.5:n.562T>A
ENST00000489643.6:n.282+284T>A
ENST00000554085.5:c.*47T>A	ENSP00000450419.1:n.*47T>A
ENST00000554139.5:n.356T>A
ENST00000554330.5:n.251T>A
ENST00000554550.5:c.252+284T>A	ENSP00000451435.1:n.252+284T>A
ENST00000554638.5:n.560T>A
ENST00000554897.5:c.252+284T>A	ENSP00000450942.1:n.252+284T>A
ENST00000554944.5:n.284T>A
ENST00000555020.5:n.333T>A
ENST00000555086.5:n.307T>A
ENST00000555214.5:n.261+284T>A
ENST00000556157.1:n.427T>A
ENST00000556244.1:c.290T>A
ENST00000556278.1:c.252+284T>A	ENSP00000451792.1:n.252+284T>A
ENST00000556403.5:n.316T>A
ENST00000556494.5:n.335T>A
ENST00000557541.5:n.447T>A
ENST00000557706.5:n.650T>A
NM_000155.3:c.303T>A	NP_000146.2:p.Ala101=
NM_001258332.1:c.50+284T>A	NP_001245261.1:n.50+284T>A
NM_000155.4:c.303T>A MANE Select	NP_000146.2:p.Ala101=
NM_001258332.2:c.50+284T>A	NP_001245261.1:n.50+284T>A