Canonical Allele Identifier: CA373278535

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647110C>A (hg19) ; chr9:g.34647113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647113C>A , CM000671.2:g.34647113C>A	GRCh38
NC_000009.11:g.34647110C>A , CM000671.1:g.34647110C>A	GRCh37
NC_000009.10:g.34637110C>A	NCBI36
NG_009029.1:g.5476C>A
NG_009029.2:g.5525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.107C>A	ENSP00000509954.1:p.Pro36Gln
ENST00000378842.8:c.107C>A MANE Select	ENSP00000368119.4:p.Pro36Gln
ENST00000378842.7:c.107C>A	ENSP00000368119.3:p.Pro36Gln
ENST00000450095.6:c.-96C>A	ENSP00000401956.2:n.-96C>A
ENST00000465543.6:n.446C>A
ENST00000468099.2:n.155-8C>A
ENST00000472111.5:n.148C>A
ENST00000473506.6:c.107C>A	ENSP00000432839.2:p.Pro36Gln
ENST00000473529.5:n.154C>A
ENST00000485531.1:n.100C>A
ENST00000487381.5:n.133C>A
ENST00000489643.6:n.137C>A
ENST00000554085.5:c.107C>A	ENSP00000450419.1:p.Pro36Gln
ENST00000554139.5:n.160C>A
ENST00000554330.5:n.104C>A
ENST00000554550.5:c.107C>A	ENSP00000451435.1:p.Pro36Gln
ENST00000554638.5:n.131C>A
ENST00000554897.5:c.107C>A	ENSP00000450942.1:p.Pro36Gln
ENST00000554944.5:n.137C>A
ENST00000555020.5:n.137C>A
ENST00000555086.5:n.111C>A
ENST00000555214.5:n.116C>A
ENST00000556157.1:n.214C>A
ENST00000556278.1:c.107C>A	ENSP00000451792.1:p.Pro36Gln
ENST00000556403.5:n.120C>A
ENST00000556494.5:n.139C>A
ENST00000557541.5:n.300C>A
ENST00000557706.5:n.221C>A
ENST00000605275.1:n.645C>A
NM_000155.3:c.107C>A	NP_000146.2:p.Pro36Gln
NM_001258332.1:c.-96C>A	NP_001245261.1:n.-96C>A
NM_000155.4:c.107C>A MANE Select	NP_000146.2:p.Pro36Gln
NM_001258332.2:c.-96C>A	NP_001245261.1:n.-96C>A