Canonical Allele Identifier: CA373284784

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649441G>C (hg19) ; chr9:g.34649444G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649444G>C , CM000671.2:g.34649444G>C	GRCh38
NC_000009.11:g.34649441G>C , CM000671.1:g.34649441G>C	GRCh37
NC_000009.10:g.34639441G>C	NCBI36
NG_009029.1:g.7807G>C
NG_028966.1:g.2260G>C
NG_009029.2:g.7856G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*527G>C	ENSP00000509954.1:n.*527G>C
ENST00000378842.8:c.939G>C MANE Select	ENSP00000368119.4:p.Trp313Cys
ENST00000378842.7:c.939G>C	ENSP00000368119.3:p.Trp313Cys
ENST00000450095.6:c.612G>C	ENSP00000401956.2:p.Trp204Cys
ENST00000488412.2:n.523G>C
ENST00000489643.6:n.1347G>C
ENST00000554550.5:c.*559G>C	ENSP00000451435.1:n.*559G>C
ENST00000554638.5:n.1411G>C
ENST00000555020.5:n.1728G>C
ENST00000555754.1:n.387G>C
ENST00000556278.1:c.432+988G>C	ENSP00000451792.1:n.432+988G>C
ENST00000557706.5:n.1514G>C
NM_000155.3:c.939G>C	NP_000146.2:p.Trp313Cys
NM_001258332.1:c.612G>C	NP_001245261.1:p.Trp204Cys
NM_000155.4:c.939G>C MANE Select	NP_000146.2:p.Trp313Cys
NM_001258332.2:c.612G>C	NP_001245261.1:p.Trp204Cys