Canonical Allele Identifier: CA373280257

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647656C>T (hg19) ; chr9:g.34647659C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647659C>T , CM000671.2:g.34647659C>T	GRCh38
NC_000009.11:g.34647656C>T , CM000671.1:g.34647656C>T	GRCh37
NC_000009.10:g.34637656C>T	NCBI36
NG_009029.1:g.6022C>T
NG_028966.1:g.475C>T
NG_009029.2:g.6071C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+92C>T	ENSP00000509954.1:n.328+92C>T
ENST00000378842.8:c.331C>T MANE Select	ENSP00000368119.4:p.Pro111Ser
ENST00000378842.7:c.331C>T	ENSP00000368119.3:p.Pro111Ser
ENST00000450095.6:c.51-173C>T	ENSP00000401956.2:n.51-173C>T
ENST00000465543.6:n.670C>T
ENST00000472111.5:n.461C>T
ENST00000473506.6:c.282C>T	ENSP00000432839.2:p.Asp94=
ENST00000473529.5:n.467C>T
ENST00000485531.1:n.646C>T
ENST00000487381.5:n.590C>T
ENST00000489643.6:n.282+401C>T
ENST00000554085.5:c.*75C>T	ENSP00000450419.1:n.*75C>T
ENST00000554139.5:n.384C>T
ENST00000554330.5:n.368C>T
ENST00000554550.5:c.253-173C>T	ENSP00000451435.1:n.253-173C>T
ENST00000554638.5:n.677C>T
ENST00000554897.5:c.253-173C>T	ENSP00000450942.1:n.253-173C>T
ENST00000554944.5:n.401C>T
ENST00000555020.5:n.361C>T
ENST00000555086.5:n.335C>T
ENST00000555214.5:n.262-389C>T
ENST00000556157.1:n.455C>T
ENST00000556244.1:c.318C>T
ENST00000556278.1:c.252+401C>T	ENSP00000451792.1:n.252+401C>T
ENST00000556403.5:n.433C>T
ENST00000556494.5:n.452C>T
ENST00000557541.5:n.475C>T
ENST00000557706.5:n.767C>T
NM_000155.3:c.331C>T	NP_000146.2:p.Pro111Ser
NM_001258332.1:c.51-173C>T	NP_001245261.1:n.51-173C>T
NM_000155.4:c.331C>T MANE Select	NP_000146.2:p.Pro111Ser
NM_001258332.2:c.51-173C>T	NP_001245261.1:n.51-173C>T