Canonical Allele Identifier: CA259425

Gene: GALT

Linked Data

• dbSNP Id: rs111033719
• MyVariant Identifiers: chr9:g.34648132_34648133insG (hg19) ; chr9:g.34648135_34648136insG (hg38)
• PubMed: PMID:8956044

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648135_34648136insG , CM000671.2:g.34648135_34648136insG	GRCh38
NC_000009.11:g.34648132_34648133insG , CM000671.1:g.34648132_34648133insG	GRCh37
NC_000009.10:g.34638132_34638133insG	NCBI36
NG_009029.1:g.6498_6499insG
NG_028966.1:g.951_952insG
NG_009029.2:g.6547_6548insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*116_*117insG	ENSP00000509954.1:n.*116_*117insG
ENST00000378842.8:c.528_529insG MANE Select	ENSP00000368119.4:p.Met177AspfsTer6
ENST00000378842.7:c.528_529insG	ENSP00000368119.3:p.Met177AspfsTer6
ENST00000450095.6:c.201_202insG	ENSP00000401956.2:p.Met68AspfsTer6
ENST00000465543.6:n.867_868insG
ENST00000472111.5:n.784_785insG
ENST00000473506.6:c.*116_*117insG	ENSP00000432839.2:n.*116_*117insG
ENST00000473529.5:n.687_688insG
ENST00000485531.1:n.1122_1123insG
ENST00000487381.5:n.913_914insG
ENST00000489643.6:n.303_304insG
ENST00000554085.5:c.*272_*273insG	ENSP00000450419.1:n.*272_*273insG
ENST00000554139.5:n.774_775insG
ENST00000554550.5:c.*148_*149insG	ENSP00000451435.1:n.*148_*149insG
ENST00000554638.5:n.1000_1001insG
ENST00000554897.5:c.*215_*216insG	ENSP00000450942.1:n.*215_*216insG
ENST00000554944.5:n.877_878insG
ENST00000555020.5:n.684_685insG
ENST00000555086.5:n.532_533insG
ENST00000555214.5:n.349_350insG
ENST00000556244.1:c.515_516insG
ENST00000556278.1:c.273_274insG	ENSP00000451792.1:p.Met92AspfsTer6
ENST00000556494.5:n.649_650insG
ENST00000557706.5:n.1090_1091insG
NM_000155.3:c.528_529insG	NP_000146.2:p.Met177AspfsTer6
NM_001258332.1:c.201_202insG	NP_001245261.1:p.Met68AspfsTer6
NM_000155.4:c.528_529insG MANE Select	NP_000146.2:p.Met177AspfsTer6
NM_001258332.2:c.201_202insG	NP_001245261.1:p.Met68AspfsTer6