Canonical Allele Identifier: CA259369

Gene: GALT

Linked Data

• dbSNP Id: rs111033677
• MyVariant Identifiers: chr9:g.34647662G>A (hg19) ; chr9:g.34647665G>A (hg38)
• PubMed: PMID:11261429

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647665G>A , CM000671.2:g.34647665G>A	GRCh38
NC_000009.11:g.34647662G>A , CM000671.1:g.34647662G>A	GRCh37
NC_000009.10:g.34637662G>A	NCBI36
NG_009029.1:g.6028G>A
NG_028966.1:g.481G>A
NG_009029.2:g.6077G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+98G>A	ENSP00000509954.1:n.328+98G>A
ENST00000378842.8:c.337G>A MANE Select	ENSP00000368119.4:p.Asp113Asn
ENST00000378842.7:c.337G>A	ENSP00000368119.3:p.Asp113Asn
ENST00000450095.6:c.51-167G>A	ENSP00000401956.2:n.51-167G>A
ENST00000465543.6:n.676G>A
ENST00000472111.5:n.467G>A
ENST00000473506.6:c.288G>A	ENSP00000432839.2:p.Val96=
ENST00000473529.5:n.473G>A
ENST00000485531.1:n.652G>A
ENST00000487381.5:n.596G>A
ENST00000489643.6:n.282+407G>A
ENST00000554085.5:c.*81G>A	ENSP00000450419.1:n.*81G>A
ENST00000554139.5:n.390G>A
ENST00000554330.5:n.374G>A
ENST00000554550.5:c.253-167G>A	ENSP00000451435.1:n.253-167G>A
ENST00000554638.5:n.683G>A
ENST00000554897.5:c.253-167G>A	ENSP00000450942.1:n.253-167G>A
ENST00000554944.5:n.407G>A
ENST00000555020.5:n.367G>A
ENST00000555086.5:n.341G>A
ENST00000555214.5:n.262-383G>A
ENST00000556157.1:n.461G>A
ENST00000556244.1:c.324G>A
ENST00000556278.1:c.252+407G>A	ENSP00000451792.1:n.252+407G>A
ENST00000556403.5:n.439G>A
ENST00000556494.5:n.458G>A
ENST00000557541.5:n.481G>A
ENST00000557706.5:n.773G>A
NM_000155.3:c.337G>A	NP_000146.2:p.Asp113Asn
NM_001258332.1:c.51-167G>A	NP_001245261.1:n.51-167G>A
NM_000155.4:c.337G>A MANE Select	NP_000146.2:p.Asp113Asn
NM_001258332.2:c.51-167G>A	NP_001245261.1:n.51-167G>A