Canonical Allele Identifier: CA2783504177

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647621_34647622insGGCACGGCC , CM000671.2:g.34647621_34647622insGGCACGGCC	GRCh38
NC_000009.11:g.34647618_34647619insGGCACGGCC , CM000671.1:g.34647618_34647619insGGCACGGCC	GRCh37
NC_000009.10:g.34637618_34637619insGGCACGGCC	NCBI36
NG_009029.1:g.5984_5985insGGCACGGCC
NG_028966.1:g.437_438insGGCACGGCC
NG_009029.2:g.6033_6034insGGCACGGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+54_328+55insGGCACGGCC	ENSP00000509954.1:n.328+54_328+55insGGCACGGCC
ENST00000378842.8:c.329-36_329-35insGGCACGGCC MANE Select	ENSP00000368119.4:n.329-36_329-35insGGCACGGCC
ENST00000378842.7:c.329-36_329-35insGGCACGGCC	ENSP00000368119.3:n.329-36_329-35insGGCACGGCC
ENST00000450095.6:c.51-211_51-210insGGCACGGCC	ENSP00000401956.2:n.51-211_51-210insGGCACGGCC
ENST00000465543.6:n.668-36_668-35insGGCACGGCC
ENST00000472111.5:n.423_424insGGCACGGCC
ENST00000473506.6:c.280-36_280-35insGGCACGGCC	ENSP00000432839.2:n.280-36_280-35insGGCACGGCC
ENST00000473529.5:n.429_430insGGCACGGCC
ENST00000485531.1:n.608_609insGGCACGGCC
ENST00000487381.5:n.588-36_588-35insGGCACGGCC
ENST00000489643.6:n.282+363_282+364insGGCACGGCC
ENST00000554085.5:c.*73-36_*73-35insGGCACGGCC	ENSP00000450419.1:n.*73-36_*73-35insGGCACGGCC
ENST00000554139.5:n.382-36_382-35insGGCACGGCC
ENST00000554330.5:n.330_331insGGCACGGCC
ENST00000554550.5:c.253-211_253-210insGGCACGGCC	ENSP00000451435.1:n.253-211_253-210insGGCACGGCC
ENST00000554638.5:n.639_640insGGCACGGCC
ENST00000554897.5:c.253-211_253-210insGGCACGGCC	ENSP00000450942.1:n.253-211_253-210insGGCACGGCC
ENST00000554944.5:n.363_364insGGCACGGCC
ENST00000555020.5:n.359-36_359-35insGGCACGGCC
ENST00000555086.5:n.333-36_333-35insGGCACGGCC
ENST00000555214.5:n.261+363_261+364insGGCACGGCC
ENST00000556157.1:n.453-36_453-35insGGCACGGCC
ENST00000556244.1:c.316-36_316-35insGGCACGGCC
ENST00000556278.1:c.252+363_252+364insGGCACGGCC	ENSP00000451792.1:n.252+363_252+364insGGCACGGCC
ENST00000556403.5:n.395_396insGGCACGGCC
ENST00000556494.5:n.414_415insGGCACGGCC
ENST00000557541.5:n.473-36_473-35insGGCACGGCC
ENST00000557706.5:n.729_730insGGCACGGCC
NM_000155.3:c.329-36_329-35insGGCACGGCC	NP_000146.2:n.329-36_329-35insGGCACGGCC
NM_001258332.1:c.51-211_51-210insGGCACGGCC	NP_001245261.1:n.51-211_51-210insGGCACGGCC
NM_000155.4:c.329-36_329-35insGGCACGGCC MANE Select	NP_000146.2:n.329-36_329-35insGGCACGGCC
NM_001258332.2:c.51-211_51-210insGGCACGGCC	NP_001245261.1:n.51-211_51-210insGGCACGGCC