Canonical Allele Identifier: CA373283888

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648843C>A (hg19) ; chr9:g.34648846C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648846C>A , CM000671.2:g.34648846C>A	GRCh38
NC_000009.11:g.34648843C>A , CM000671.1:g.34648843C>A	GRCh37
NC_000009.10:g.34638843C>A	NCBI36
NG_028966.1:g.1662C>A
NG_009029.2:g.7258C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*360C>A	ENSP00000509954.1:n.*360C>A
ENST00000378842.8:c.772C>A MANE Select	ENSP00000368119.4:p.Arg258Ser
ENST00000378842.7:c.772C>A	ENSP00000368119.3:p.Arg258Ser
ENST00000450095.6:c.445C>A	ENSP00000401956.2:p.Arg149Ser
ENST00000473506.6:c.*360C>A	ENSP00000432839.2:n.*360C>A
ENST00000489643.6:n.852C>A
ENST00000554085.5:c.*516C>A	ENSP00000450419.1:n.*516C>A
ENST00000554550.5:c.*392C>A	ENSP00000451435.1:n.*392C>A
ENST00000554638.5:n.1244C>A
ENST00000555020.5:n.1233C>A
ENST00000555086.5:n.776C>A
ENST00000555754.1:n.117C>A
ENST00000556244.1:c.759C>A
ENST00000556278.1:c.432+390C>A	ENSP00000451792.1:n.432+390C>A
ENST00000557706.5:n.1334C>A
NM_000155.3:c.772C>A	NP_000146.2:p.Arg258Ser
NM_001258332.1:c.445C>A	NP_001245261.1:p.Arg149Ser
NM_000155.4:c.772C>A MANE Select	NP_000146.2:p.Arg258Ser
NM_001258332.2:c.445C>A	NP_001245261.1:p.Arg149Ser