Canonical Allele Identifier: CA373279132

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647505A>T (hg19) ; chr9:g.34647508A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647508A>T , CM000671.2:g.34647508A>T	GRCh38
NC_000009.11:g.34647505A>T , CM000671.1:g.34647505A>T	GRCh37
NC_000009.10:g.34637505A>T	NCBI36
NG_009029.1:g.5871A>T
NG_028966.1:g.324A>T
NG_009029.2:g.5920A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.269A>T	ENSP00000509954.1:p.Asp90Val
ENST00000378842.8:c.269A>T MANE Select	ENSP00000368119.4:p.Asp90Val
ENST00000378842.7:c.269A>T	ENSP00000368119.3:p.Asp90Val
ENST00000450095.6:c.50+250A>T	ENSP00000401956.2:n.50+250A>T
ENST00000465543.6:n.608A>T
ENST00000468099.2:n.542A>T
ENST00000472111.5:n.310A>T
ENST00000473506.6:c.253-33A>T	ENSP00000432839.2:n.253-33A>T
ENST00000473529.5:n.316A>T
ENST00000485531.1:n.495A>T
ENST00000487381.5:n.528A>T
ENST00000489643.6:n.282+250A>T
ENST00000554085.5:c.*13A>T	ENSP00000450419.1:n.*13A>T
ENST00000554139.5:n.322A>T
ENST00000554330.5:n.250-33A>T
ENST00000554550.5:c.252+250A>T	ENSP00000451435.1:n.252+250A>T
ENST00000554638.5:n.526A>T
ENST00000554897.5:c.252+250A>T	ENSP00000450942.1:n.252+250A>T
ENST00000554944.5:n.283-33A>T
ENST00000555020.5:n.299A>T
ENST00000555086.5:n.273A>T
ENST00000555214.5:n.261+250A>T
ENST00000556157.1:n.393A>T
ENST00000556244.1:c.256A>T
ENST00000556278.1:c.252+250A>T	ENSP00000451792.1:n.252+250A>T
ENST00000556403.5:n.282A>T
ENST00000556494.5:n.301A>T
ENST00000557541.5:n.446-33A>T
ENST00000557706.5:n.616A>T
NM_000155.3:c.269A>T	NP_000146.2:p.Asp90Val
NM_001258332.1:c.50+250A>T	NP_001245261.1:n.50+250A>T
NM_000155.4:c.269A>T MANE Select	NP_000146.2:p.Asp90Val
NM_001258332.2:c.50+250A>T	NP_001245261.1:n.50+250A>T