Canonical Allele Identifier: CA1845636452

Gene: GALT

Linked Data

• dbSNP Id: rs1587238078

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647646C>T , CM000671.2:g.34647646C>T	GRCh38
NC_000009.11:g.34647643C>T , CM000671.1:g.34647643C>T	GRCh37
NC_000009.10:g.34637643C>T	NCBI36
NG_009029.1:g.6009C>T
NG_028966.1:g.462C>T
NG_009029.2:g.6058C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+79C>T	ENSP00000509954.1:n.328+79C>T
ENST00000378842.8:c.329-11C>T MANE Select	ENSP00000368119.4:n.329-11C>T
ENST00000378842.7:c.329-11C>T	ENSP00000368119.3:n.329-11C>T
ENST00000450095.6:c.51-186C>T	ENSP00000401956.2:n.51-186C>T
ENST00000465543.6:n.668-11C>T
ENST00000472111.5:n.448C>T
ENST00000473506.6:c.280-11C>T	ENSP00000432839.2:n.280-11C>T
ENST00000473529.5:n.454C>T
ENST00000485531.1:n.633C>T
ENST00000487381.5:n.588-11C>T
ENST00000489643.6:n.282+388C>T
ENST00000554085.5:c.*73-11C>T	ENSP00000450419.1:n.*73-11C>T
ENST00000554139.5:n.382-11C>T
ENST00000554330.5:n.355C>T
ENST00000554550.5:c.253-186C>T	ENSP00000451435.1:n.253-186C>T
ENST00000554638.5:n.664C>T
ENST00000554897.5:c.253-186C>T	ENSP00000450942.1:n.253-186C>T
ENST00000554944.5:n.388C>T
ENST00000555020.5:n.359-11C>T
ENST00000555086.5:n.333-11C>T
ENST00000555214.5:n.261+388C>T
ENST00000556157.1:n.453-11C>T
ENST00000556244.1:c.316-11C>T
ENST00000556278.1:c.252+388C>T	ENSP00000451792.1:n.252+388C>T
ENST00000556403.5:n.420C>T
ENST00000556494.5:n.439C>T
ENST00000557541.5:n.473-11C>T
ENST00000557706.5:n.754C>T
NM_000155.3:c.329-11C>T	NP_000146.2:n.329-11C>T
NM_001258332.1:c.51-186C>T	NP_001245261.1:n.51-186C>T
NM_000155.4:c.329-11C>T MANE Select	NP_000146.2:n.329-11C>T
NM_001258332.2:c.51-186C>T	NP_001245261.1:n.51-186C>T