Canonical Allele Identifier: CA373280088

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647551T>A (hg19) ; chr9:g.34647554T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647554T>A , CM000671.2:g.34647554T>A	GRCh38
NC_000009.11:g.34647551T>A , CM000671.1:g.34647551T>A	GRCh37
NC_000009.10:g.34637551T>A	NCBI36
NG_009029.1:g.5917T>A
NG_028966.1:g.370T>A
NG_009029.2:g.5966T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.315T>A	ENSP00000509954.1:p.Asp105Glu
ENST00000378842.8:c.315T>A MANE Select	ENSP00000368119.4:p.Asp105Glu
ENST00000378842.7:c.315T>A	ENSP00000368119.3:p.Asp105Glu
ENST00000450095.6:c.51-278T>A	ENSP00000401956.2:n.51-278T>A
ENST00000465543.6:n.654T>A
ENST00000472111.5:n.356T>A
ENST00000473506.6:c.266T>A	ENSP00000432839.2:p.Met89Lys
ENST00000473529.5:n.362T>A
ENST00000485531.1:n.541T>A
ENST00000487381.5:n.574T>A
ENST00000489643.6:n.282+296T>A
ENST00000554085.5:c.*59T>A	ENSP00000450419.1:n.*59T>A
ENST00000554139.5:n.368T>A
ENST00000554330.5:n.263T>A
ENST00000554550.5:c.253-278T>A	ENSP00000451435.1:n.253-278T>A
ENST00000554638.5:n.572T>A
ENST00000554897.5:c.253-278T>A	ENSP00000450942.1:n.253-278T>A
ENST00000554944.5:n.296T>A
ENST00000555020.5:n.345T>A
ENST00000555086.5:n.319T>A
ENST00000555214.5:n.261+296T>A
ENST00000556157.1:n.439T>A
ENST00000556244.1:c.302T>A
ENST00000556278.1:c.252+296T>A	ENSP00000451792.1:n.252+296T>A
ENST00000556403.5:n.328T>A
ENST00000556494.5:n.347T>A
ENST00000557541.5:n.459T>A
ENST00000557706.5:n.662T>A
NM_000155.3:c.315T>A	NP_000146.2:p.Asp105Glu
NM_001258332.1:c.51-278T>A	NP_001245261.1:n.51-278T>A
NM_000155.4:c.315T>A MANE Select	NP_000146.2:p.Asp105Glu
NM_001258332.2:c.51-278T>A	NP_001245261.1:n.51-278T>A