Canonical Allele Identifier: CA2719562136

Gene: GALT

Linked Data

• dbSNP Id: rs2132341865

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647262_34647263insTCCCCA , CM000671.2:g.34647262_34647263insTCCCCA	GRCh38
NC_000009.11:g.34647259_34647260insTCCCCA , CM000671.1:g.34647259_34647260insTCCCCA	GRCh37
NC_000009.10:g.34637259_34637260insTCCCCA	NCBI36
NG_009029.1:g.5625_5626insTCCCCA
NG_028966.1:g.78_79insTCCCCA
NG_009029.2:g.5674_5675insTCCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.252+4_252+5insTCCCCA	ENSP00000509954.1:n.252+4_252+5insTCCCCA
ENST00000378842.8:c.252+4_252+5insTCCCCA MANE Select	ENSP00000368119.4:n.252+4_252+5insTCCCCA
ENST00000378842.7:c.252+4_252+5insTCCCCA	ENSP00000368119.3:n.252+4_252+5insTCCCCA
ENST00000450095.6:c.50+4_50+5insTCCCCA	ENSP00000401956.2:n.50+4_50+5insTCCCCA
ENST00000465543.6:n.591+4_591+5insTCCCCA
ENST00000468099.2:n.296_297insTCCCCA
ENST00000472111.5:n.293+4_293+5insTCCCCA
ENST00000473506.6:c.252+4_252+5insTCCCCA	ENSP00000432839.2:n.252+4_252+5insTCCCCA
ENST00000473529.5:n.299+4_299+5insTCCCCA
ENST00000485531.1:n.249_250insTCCCCA
ENST00000487381.5:n.282_283insTCCCCA
ENST00000489643.6:n.282+4_282+5insTCCCCA
ENST00000554085.5:c.252+4_252+5insTCCCCA	ENSP00000450419.1:n.252+4_252+5insTCCCCA
ENST00000554139.5:n.305+4_305+5insTCCCCA
ENST00000554330.5:n.249+4_249+5insTCCCCA
ENST00000554550.5:c.252+4_252+5insTCCCCA	ENSP00000451435.1:n.252+4_252+5insTCCCCA
ENST00000554638.5:n.280_281insTCCCCA
ENST00000554897.5:c.252+4_252+5insTCCCCA	ENSP00000450942.1:n.252+4_252+5insTCCCCA
ENST00000554944.5:n.282+4_282+5insTCCCCA
ENST00000555020.5:n.282+4_282+5insTCCCCA
ENST00000555086.5:n.256+4_256+5insTCCCCA
ENST00000555214.5:n.261+4_261+5insTCCCCA
ENST00000556157.1:n.359+4_359+5insTCCCCA
ENST00000556244.1:c.136+4_136+5insTCCCCA
ENST00000556278.1:c.252+4_252+5insTCCCCA	ENSP00000451792.1:n.252+4_252+5insTCCCCA
ENST00000556403.5:n.265+4_265+5insTCCCCA
ENST00000556494.5:n.284+4_284+5insTCCCCA
ENST00000557541.5:n.445+4_445+5insTCCCCA
ENST00000557706.5:n.370_371insTCCCCA
NM_000155.3:c.252+4_252+5insTCCCCA	NP_000146.2:n.252+4_252+5insTCCCCA
NM_001258332.1:c.50+4_50+5insTCCCCA	NP_001245261.1:n.50+4_50+5insTCCCCA
NM_000155.4:c.252+4_252+5insTCCCCA MANE Select	NP_000146.2:n.252+4_252+5insTCCCCA
NM_001258332.2:c.50+4_50+5insTCCCCA	NP_001245261.1:n.50+4_50+5insTCCCCA