Canonical Allele Identifier: CA2719561763

Gene: GALT

Linked Data

• dbSNP Id: rs2132341849

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647260_34647261insG , CM000671.2:g.34647260_34647261insG	GRCh38
NC_000009.11:g.34647257_34647258insG , CM000671.1:g.34647257_34647258insG	GRCh37
NC_000009.10:g.34637257_34637258insG	NCBI36
NG_009029.1:g.5623_5624insG
NG_028966.1:g.76_77insG
NG_009029.2:g.5672_5673insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.252+2_252+3insG	ENSP00000509954.1:n.252+2_252+3insG
ENST00000378842.8:c.252+2_252+3insG MANE Select	ENSP00000368119.4:n.252+2_252+3insG
ENST00000378842.7:c.252+2_252+3insG	ENSP00000368119.3:n.252+2_252+3insG
ENST00000450095.6:c.50+2_50+3insG	ENSP00000401956.2:n.50+2_50+3insG
ENST00000465543.6:n.591+2_591+3insG
ENST00000468099.2:n.294_295insG
ENST00000472111.5:n.293+2_293+3insG
ENST00000473506.6:c.252+2_252+3insG	ENSP00000432839.2:n.252+2_252+3insG
ENST00000473529.5:n.299+2_299+3insG
ENST00000485531.1:n.247_248insG
ENST00000487381.5:n.280_281insG
ENST00000489643.6:n.282+2_282+3insG
ENST00000554085.5:c.252+2_252+3insG	ENSP00000450419.1:n.252+2_252+3insG
ENST00000554139.5:n.305+2_305+3insG
ENST00000554330.5:n.249+2_249+3insG
ENST00000554550.5:c.252+2_252+3insG	ENSP00000451435.1:n.252+2_252+3insG
ENST00000554638.5:n.278_279insG
ENST00000554897.5:c.252+2_252+3insG	ENSP00000450942.1:n.252+2_252+3insG
ENST00000554944.5:n.282+2_282+3insG
ENST00000555020.5:n.282+2_282+3insG
ENST00000555086.5:n.256+2_256+3insG
ENST00000555214.5:n.261+2_261+3insG
ENST00000556157.1:n.359+2_359+3insG
ENST00000556244.1:c.136+2_136+3insG
ENST00000556278.1:c.252+2_252+3insG	ENSP00000451792.1:n.252+2_252+3insG
ENST00000556403.5:n.265+2_265+3insG
ENST00000556494.5:n.284+2_284+3insG
ENST00000557541.5:n.445+2_445+3insG
ENST00000557706.5:n.368_369insG
NM_000155.3:c.252+2_252+3insG	NP_000146.2:n.252+2_252+3insG
NM_001258332.1:c.50+2_50+3insG	NP_001245261.1:n.50+2_50+3insG
NM_000155.4:c.252+2_252+3insG MANE Select	NP_000146.2:n.252+2_252+3insG
NM_001258332.2:c.50+2_50+3insG	NP_001245261.1:n.50+2_50+3insG