Canonical Allele Identifier: CA373282279

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648427T>G (hg19) ; chr9:g.34648430T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648430T>G , CM000671.2:g.34648430T>G	GRCh38
NC_000009.11:g.34648427T>G , CM000671.1:g.34648427T>G	GRCh37
NC_000009.10:g.34638427T>G	NCBI36
NG_009029.1:g.6793T>G
NG_028966.1:g.1246T>G
NG_009029.2:g.6842T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*249T>G	ENSP00000509954.1:n.*249T>G
ENST00000378842.8:c.661T>G MANE Select	ENSP00000368119.4:p.Tyr221Asp
ENST00000378842.7:c.661T>G	ENSP00000368119.3:p.Tyr221Asp
ENST00000450095.6:c.334T>G	ENSP00000401956.2:p.Tyr112Asp
ENST00000472111.5:n.917T>G
ENST00000473506.6:c.*249T>G	ENSP00000432839.2:n.*249T>G
ENST00000473529.5:n.820T>G
ENST00000487381.5:n.1046T>G
ENST00000489643.6:n.436T>G
ENST00000554085.5:c.*405T>G	ENSP00000450419.1:n.*405T>G
ENST00000554550.5:c.*281T>G	ENSP00000451435.1:n.*281T>G
ENST00000554638.5:n.1133T>G
ENST00000555020.5:n.817T>G
ENST00000555086.5:n.665T>G
ENST00000555214.5:n.482T>G
ENST00000555754.1:n.6T>G
ENST00000556244.1:c.648T>G
ENST00000556278.1:c.406T>G	ENSP00000451792.1:p.Tyr136Asp
ENST00000556494.5:n.782T>G
ENST00000557706.5:n.1223T>G
NM_000155.3:c.661T>G	NP_000146.2:p.Tyr221Asp
NM_001258332.1:c.334T>G	NP_001245261.1:p.Tyr112Asp
NM_000155.4:c.661T>G MANE Select	NP_000146.2:p.Tyr221Asp
NM_001258332.2:c.334T>G	NP_001245261.1:p.Tyr112Asp