Canonical Allele Identifier: CA373278488

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647095A>C (hg19) ; chr9:g.34647098A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647098A>C , CM000671.2:g.34647098A>C	GRCh38
NC_000009.11:g.34647095A>C , CM000671.1:g.34647095A>C	GRCh37
NC_000009.10:g.34637095A>C	NCBI36
NG_009029.1:g.5461A>C
NG_009029.2:g.5510A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.92A>C	ENSP00000509954.1:p.His31Pro
ENST00000378842.8:c.92A>C MANE Select	ENSP00000368119.4:p.His31Pro
ENST00000378842.7:c.92A>C	ENSP00000368119.3:p.His31Pro
ENST00000450095.6:c.-111A>C	ENSP00000401956.2:n.-111A>C
ENST00000465543.6:n.431A>C
ENST00000468099.2:n.155-23A>C
ENST00000472111.5:n.133A>C
ENST00000473506.6:c.92A>C	ENSP00000432839.2:p.His31Pro
ENST00000473529.5:n.139A>C
ENST00000485531.1:n.85A>C
ENST00000487381.5:n.118A>C
ENST00000489643.6:n.122A>C
ENST00000554085.5:c.92A>C	ENSP00000450419.1:p.His31Pro
ENST00000554139.5:n.145A>C
ENST00000554330.5:n.89A>C
ENST00000554550.5:c.92A>C	ENSP00000451435.1:p.His31Pro
ENST00000554638.5:n.116A>C
ENST00000554897.5:c.92A>C	ENSP00000450942.1:p.His31Pro
ENST00000554944.5:n.122A>C
ENST00000555020.5:n.122A>C
ENST00000555086.5:n.96A>C
ENST00000555214.5:n.101A>C
ENST00000556157.1:n.199A>C
ENST00000556278.1:c.92A>C	ENSP00000451792.1:p.His31Pro
ENST00000556403.5:n.105A>C
ENST00000556494.5:n.124A>C
ENST00000557541.5:n.285A>C
ENST00000557706.5:n.206A>C
ENST00000605275.1:n.630A>C
NM_000155.3:c.92A>C	NP_000146.2:p.His31Pro
NM_001258332.1:c.-111A>C	NP_001245261.1:n.-111A>C
NM_000155.4:c.92A>C MANE Select	NP_000146.2:p.His31Pro
NM_001258332.2:c.-111A>C	NP_001245261.1:n.-111A>C