Canonical Allele Identifier: CA373284769

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649439T>A (hg19) ; chr9:g.34649442T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649442T>A , CM000671.2:g.34649442T>A	GRCh38
NC_000009.11:g.34649439T>A , CM000671.1:g.34649439T>A	GRCh37
NC_000009.10:g.34639439T>A	NCBI36
NG_009029.1:g.7805T>A
NG_028966.1:g.2258T>A
NG_009029.2:g.7854T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*525T>A	ENSP00000509954.1:n.*525T>A
ENST00000378842.8:c.937T>A MANE Select	ENSP00000368119.4:p.Trp313Arg
ENST00000378842.7:c.937T>A	ENSP00000368119.3:p.Trp313Arg
ENST00000450095.6:c.610T>A	ENSP00000401956.2:p.Trp204Arg
ENST00000488412.2:n.521T>A
ENST00000489643.6:n.1345T>A
ENST00000554550.5:c.*557T>A	ENSP00000451435.1:n.*557T>A
ENST00000554638.5:n.1409T>A
ENST00000555020.5:n.1726T>A
ENST00000555754.1:n.385T>A
ENST00000556278.1:c.432+986T>A	ENSP00000451792.1:n.432+986T>A
ENST00000557706.5:n.1512T>A
NM_000155.3:c.937T>A	NP_000146.2:p.Trp313Arg
NM_001258332.1:c.610T>A	NP_001245261.1:p.Trp204Arg
NM_000155.4:c.937T>A MANE Select	NP_000146.2:p.Trp313Arg
NM_001258332.2:c.610T>A	NP_001245261.1:p.Trp204Arg