Canonical Allele Identifier: CA1845636394

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647613_34647615delinsCTT , CM000671.2:g.34647613_34647615delinsCTT	GRCh38
NC_000009.11:g.34647610_34647612delinsCTT , CM000671.1:g.34647610_34647612delinsCTT	GRCh37
NC_000009.10:g.34637610_34637612delinsCTT	NCBI36
NG_009029.1:g.5976_5978delinsCTT
NG_028966.1:g.429_431delinsCTT
NG_009029.2:g.6025_6027delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+46_328+48delinsCTT	ENSP00000509954.1:n.328+46_328+48delinsCTT
ENST00000378842.8:c.329-44_329-42delinsCTT MANE Select	ENSP00000368119.4:n.329-44_329-42delinsCTT
ENST00000378842.7:c.329-44_329-42delinsCTT	ENSP00000368119.3:n.329-44_329-42delinsCTT
ENST00000450095.6:c.51-219_51-217delinsCTT	ENSP00000401956.2:n.51-219_51-217delinsCTT
ENST00000465543.6:n.668-44_668-42delinsCTT
ENST00000472111.5:n.415_417delinsCTT
ENST00000473506.6:c.280-44_280-42delinsCTT	ENSP00000432839.2:n.280-44_280-42delinsCTT
ENST00000473529.5:n.421_423delinsCTT
ENST00000485531.1:n.600_602delinsCTT
ENST00000487381.5:n.588-44_588-42delinsCTT
ENST00000489643.6:n.282+355_282+357delinsCTT
ENST00000554085.5:c.*73-44_*73-42delinsCTT	ENSP00000450419.1:n.*73-44_*73-42delinsCTT
ENST00000554139.5:n.382-44_382-42delinsCTT
ENST00000554330.5:n.322_324delinsCTT
ENST00000554550.5:c.253-219_253-217delinsCTT	ENSP00000451435.1:n.253-219_253-217delinsCTT
ENST00000554638.5:n.631_633delinsCTT
ENST00000554897.5:c.253-219_253-217delinsCTT	ENSP00000450942.1:n.253-219_253-217delinsCTT
ENST00000554944.5:n.355_357delinsCTT
ENST00000555020.5:n.359-44_359-42delinsCTT
ENST00000555086.5:n.333-44_333-42delinsCTT
ENST00000555214.5:n.261+355_261+357delinsCTT
ENST00000556157.1:n.453-44_453-42delinsCTT
ENST00000556244.1:c.316-44_316-42delinsCTT
ENST00000556278.1:c.252+355_252+357delinsCTT	ENSP00000451792.1:n.252+355_252+357delinsCTT
ENST00000556403.5:n.387_389delinsCTT
ENST00000556494.5:n.406_408delinsCTT
ENST00000557541.5:n.473-44_473-42delinsCTT
ENST00000557706.5:n.721_723delinsCTT
NM_000155.3:c.329-44_329-42delinsCTT	NP_000146.2:n.329-44_329-42delinsCTT
NM_001258332.1:c.51-219_51-217delinsCTT	NP_001245261.1:n.51-219_51-217delinsCTT
NM_000155.4:c.329-44_329-42delinsCTT MANE Select	NP_000146.2:n.329-44_329-42delinsCTT
NM_001258332.2:c.51-219_51-217delinsCTT	NP_001245261.1:n.51-219_51-217delinsCTT