Canonical Allele Identifier: CA373278626

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647155G>C (hg19) ; chr9:g.34647158G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647158G>C , CM000671.2:g.34647158G>C	GRCh38
NC_000009.11:g.34647155G>C , CM000671.1:g.34647155G>C	GRCh37
NC_000009.10:g.34637155G>C	NCBI36
NG_009029.1:g.5521G>C
NG_009029.2:g.5570G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.152G>C	ENSP00000509954.1:p.Arg51Pro
ENST00000378842.8:c.152G>C MANE Select	ENSP00000368119.4:p.Arg51Pro
ENST00000378842.7:c.152G>C	ENSP00000368119.3:p.Arg51Pro
ENST00000450095.6:c.-51G>C	ENSP00000401956.2:n.-51G>C
ENST00000465543.6:n.491G>C
ENST00000468099.2:n.192G>C
ENST00000472111.5:n.193G>C
ENST00000473506.6:c.152G>C	ENSP00000432839.2:p.Arg51Pro
ENST00000473529.5:n.199G>C
ENST00000485531.1:n.145G>C
ENST00000487381.5:n.178G>C
ENST00000489643.6:n.182G>C
ENST00000554085.5:c.152G>C	ENSP00000450419.1:p.Arg51Pro
ENST00000554139.5:n.205G>C
ENST00000554330.5:n.149G>C
ENST00000554550.5:c.152G>C	ENSP00000451435.1:p.Arg51Pro
ENST00000554638.5:n.176G>C
ENST00000554897.5:c.152G>C	ENSP00000450942.1:p.Arg51Pro
ENST00000554944.5:n.182G>C
ENST00000555020.5:n.182G>C
ENST00000555086.5:n.156G>C
ENST00000555214.5:n.161G>C
ENST00000556157.1:n.259G>C
ENST00000556244.1:c.36G>C
ENST00000556278.1:c.152G>C	ENSP00000451792.1:p.Arg51Pro
ENST00000556403.5:n.165G>C
ENST00000556494.5:n.184G>C
ENST00000557541.5:n.345G>C
ENST00000557706.5:n.266G>C
NM_000155.3:c.152G>C	NP_000146.2:p.Arg51Pro
NM_001258332.1:c.-51G>C	NP_001245261.1:n.-51G>C
NM_000155.4:c.152G>C MANE Select	NP_000146.2:p.Arg51Pro
NM_001258332.2:c.-51G>C	NP_001245261.1:n.-51G>C