Canonical Allele Identifier: CA1845636425

Gene: GALT

Linked Data

• dbSNP Id: rs1821139195

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647634A>G , CM000671.2:g.34647634A>G	GRCh38
NC_000009.11:g.34647631A>G , CM000671.1:g.34647631A>G	GRCh37
NC_000009.10:g.34637631A>G	NCBI36
NG_009029.1:g.5997A>G
NG_028966.1:g.450A>G
NG_009029.2:g.6046A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+67A>G	ENSP00000509954.1:n.328+67A>G
ENST00000378842.8:c.329-23A>G MANE Select	ENSP00000368119.4:n.329-23A>G
ENST00000378842.7:c.329-23A>G	ENSP00000368119.3:n.329-23A>G
ENST00000450095.6:c.51-198A>G	ENSP00000401956.2:n.51-198A>G
ENST00000465543.6:n.668-23A>G
ENST00000472111.5:n.436A>G
ENST00000473506.6:c.280-23A>G	ENSP00000432839.2:n.280-23A>G
ENST00000473529.5:n.442A>G
ENST00000485531.1:n.621A>G
ENST00000487381.5:n.588-23A>G
ENST00000489643.6:n.282+376A>G
ENST00000554085.5:c.*73-23A>G	ENSP00000450419.1:n.*73-23A>G
ENST00000554139.5:n.382-23A>G
ENST00000554330.5:n.343A>G
ENST00000554550.5:c.253-198A>G	ENSP00000451435.1:n.253-198A>G
ENST00000554638.5:n.652A>G
ENST00000554897.5:c.253-198A>G	ENSP00000450942.1:n.253-198A>G
ENST00000554944.5:n.376A>G
ENST00000555020.5:n.359-23A>G
ENST00000555086.5:n.333-23A>G
ENST00000555214.5:n.261+376A>G
ENST00000556157.1:n.453-23A>G
ENST00000556244.1:c.316-23A>G
ENST00000556278.1:c.252+376A>G	ENSP00000451792.1:n.252+376A>G
ENST00000556403.5:n.408A>G
ENST00000556494.5:n.427A>G
ENST00000557541.5:n.473-23A>G
ENST00000557706.5:n.742A>G
NM_000155.3:c.329-23A>G	NP_000146.2:n.329-23A>G
NM_001258332.1:c.51-198A>G	NP_001245261.1:n.51-198A>G
NM_000155.4:c.329-23A>G MANE Select	NP_000146.2:n.329-23A>G
NM_001258332.2:c.51-198A>G	NP_001245261.1:n.51-198A>G