Canonical Allele Identifier: CA2783504178

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647623_34647624insGCAGATTTTCCAGCGGATCCCCCGGTGGCC , CM000671.2:g.34647623_34647624insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	GRCh38
NC_000009.11:g.34647620_34647621insGCAGATTTTCCAGCGGATCCCCCGGTGGCC , CM000671.1:g.34647620_34647621insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	GRCh37
NC_000009.10:g.34637620_34637621insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	NCBI36
NG_009029.1:g.5986_5987insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
NG_028966.1:g.439_440insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
NG_009029.2:g.6035_6036insGCAGATTTTCCAGCGGATCCCCCGGTGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+56_328+57insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000509954.1:n.328+56_328+57insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000378842.8:c.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC MANE Select	ENSP00000368119.4:n.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000378842.7:c.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000368119.3:n.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000450095.6:c.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000401956.2:n.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000465543.6:n.668-34_668-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000472111.5:n.425_426insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000473506.6:c.280-34_280-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000432839.2:n.280-34_280-33insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000473529.5:n.431_432insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000485531.1:n.610_611insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000487381.5:n.588-34_588-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000489643.6:n.282+365_282+366insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000554085.5:c.*73-34_*73-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000450419.1:n.*73-34_*73-33insGCAGATTTTCCAGCGGATCCCCCGG...
ENST00000554139.5:n.382-34_382-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000554330.5:n.332_333insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000554550.5:c.253-209_253-208insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000451435.1:n.253-209_253-208insGCAGATTTTCCAGCGGATCCCCC...
ENST00000554638.5:n.641_642insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000554897.5:c.253-209_253-208insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000450942.1:n.253-209_253-208insGCAGATTTTCCAGCGGATCCCCC...
ENST00000554944.5:n.365_366insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000555020.5:n.359-34_359-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000555086.5:n.333-34_333-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000555214.5:n.261+365_261+366insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000556157.1:n.453-34_453-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000556244.1:c.316-34_316-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000556278.1:c.252+365_252+366insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	ENSP00000451792.1:n.252+365_252+366insGCAGATTTTCCAGCGGATCCCCC...
ENST00000556403.5:n.397_398insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000556494.5:n.416_417insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000557541.5:n.473-34_473-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
ENST00000557706.5:n.731_732insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
NM_000155.3:c.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	NP_000146.2:n.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
NM_001258332.1:c.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	NP_001245261.1:n.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGGTGG...
NM_000155.4:c.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC MANE Select	NP_000146.2:n.329-34_329-33insGCAGATTTTCCAGCGGATCCCCCGGTGGCC
NM_001258332.2:c.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGGTGGCC	NP_001245261.1:n.51-209_51-208insGCAGATTTTCCAGCGGATCCCCCGGTGG...