Canonical Allele Identifier: CA373282185

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648407G>T (hg19) ; chr9:g.34648410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648410G>T , CM000671.2:g.34648410G>T	GRCh38
NC_000009.11:g.34648407G>T , CM000671.1:g.34648407G>T	GRCh37
NC_000009.10:g.34638407G>T	NCBI36
NG_009029.1:g.6773G>T
NG_028966.1:g.1226G>T
NG_009029.2:g.6822G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*229G>T	ENSP00000509954.1:n.*229G>T
ENST00000378842.8:c.641G>T MANE Select	ENSP00000368119.4:p.Gly214Val
ENST00000378842.7:c.641G>T	ENSP00000368119.3:p.Gly214Val
ENST00000450095.6:c.314G>T	ENSP00000401956.2:p.Gly105Val
ENST00000472111.5:n.897G>T
ENST00000473506.6:c.*229G>T	ENSP00000432839.2:n.*229G>T
ENST00000473529.5:n.800G>T
ENST00000487381.5:n.1026G>T
ENST00000489643.6:n.416G>T
ENST00000554085.5:c.*385G>T	ENSP00000450419.1:n.*385G>T
ENST00000554550.5:c.*261G>T	ENSP00000451435.1:n.*261G>T
ENST00000554638.5:n.1113G>T
ENST00000555020.5:n.797G>T
ENST00000555086.5:n.645G>T
ENST00000555214.5:n.462G>T
ENST00000556244.1:c.628G>T
ENST00000556278.1:c.386G>T	ENSP00000451792.1:p.Gly129Val
ENST00000556494.5:n.762G>T
ENST00000557706.5:n.1203G>T
NM_000155.3:c.641G>T	NP_000146.2:p.Gly214Val
NM_001258332.1:c.314G>T	NP_001245261.1:p.Gly105Val
NM_000155.4:c.641G>T MANE Select	NP_000146.2:p.Gly214Val
NM_001258332.2:c.314G>T	NP_001245261.1:p.Gly105Val