Canonical Allele Identifier: CA464402170

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648390C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648393C>T , CM000671.2:g.34648393C>T	GRCh38
NC_000009.11:g.34648390C>T , CM000671.1:g.34648390C>T	GRCh37
NC_000009.10:g.34638390C>T	NCBI36
NG_009029.1:g.6756C>T
NG_028966.1:g.1209C>T
NG_009029.2:g.6805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*212C>T	ENSP00000509954.1:n.*212C>T
ENST00000378842.8:c.624C>T MANE Select	ENSP00000368119.4:p.Ala208=
ENST00000378842.7:c.624C>T	ENSP00000368119.3:p.Ala208=
ENST00000450095.6:c.297C>T	ENSP00000401956.2:p.Ala99=
ENST00000472111.5:n.880C>T
ENST00000473506.6:c.*212C>T	ENSP00000432839.2:n.*212C>T
ENST00000473529.5:n.783C>T
ENST00000487381.5:n.1009C>T
ENST00000489643.6:n.399C>T
ENST00000554085.5:c.*368C>T	ENSP00000450419.1:n.*368C>T
ENST00000554550.5:c.*244C>T	ENSP00000451435.1:n.*244C>T
ENST00000554638.5:n.1096C>T
ENST00000555020.5:n.780C>T
ENST00000555086.5:n.628C>T
ENST00000555214.5:n.445C>T
ENST00000556244.1:c.611C>T
ENST00000556278.1:c.369C>T	ENSP00000451792.1:p.Ala123=
ENST00000556494.5:n.745C>T
ENST00000557706.5:n.1186C>T
NM_000155.3:c.624C>T	NP_000146.2:p.Ala208=
NM_001258332.1:c.297C>T	NP_001245261.1:p.Ala99=
NM_000155.4:c.624C>T MANE Select	NP_000146.2:p.Ala208=
NM_001258332.2:c.297C>T	NP_001245261.1:p.Ala99=