Canonical Allele Identifier: CA373283900

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648847G>C (hg19) ; chr9:g.34648850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648850G>C , CM000671.2:g.34648850G>C	GRCh38
NC_000009.11:g.34648847G>C , CM000671.1:g.34648847G>C	GRCh37
NC_000009.10:g.34638847G>C	NCBI36
NG_009029.1:g.7212G>C
NG_028966.1:g.1666G>C
NG_009029.2:g.7262G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*364G>C	ENSP00000509954.1:n.*364G>C
ENST00000378842.8:c.776G>C MANE Select	ENSP00000368119.4:p.Arg259Pro
ENST00000378842.7:c.776G>C	ENSP00000368119.3:p.Arg259Pro
ENST00000450095.6:c.449G>C	ENSP00000401956.2:p.Arg150Pro
ENST00000473506.6:c.*364G>C	ENSP00000432839.2:n.*364G>C
ENST00000489643.6:n.856G>C
ENST00000554085.5:c.*520G>C	ENSP00000450419.1:n.*520G>C
ENST00000554550.5:c.*396G>C	ENSP00000451435.1:n.*396G>C
ENST00000554638.5:n.1248G>C
ENST00000555020.5:n.1237G>C
ENST00000555086.5:n.780G>C
ENST00000555754.1:n.121G>C
ENST00000556244.1:c.763G>C
ENST00000556278.1:c.432+394G>C	ENSP00000451792.1:n.432+394G>C
ENST00000557706.5:n.1338G>C
NM_000155.3:c.776G>C	NP_000146.2:p.Arg259Pro
NM_001258332.1:c.449G>C	NP_001245261.1:p.Arg150Pro
NM_000155.4:c.776G>C MANE Select	NP_000146.2:p.Arg259Pro
NM_001258332.2:c.449G>C	NP_001245261.1:p.Arg150Pro