Canonical Allele Identifier: CA2738226524

Gene: ALG12

Linked Data

• dbSNP Id: rs2146615454

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.49914000_49914006dup , CM000684.2:g.49914000_49914006dup	GRCh38
NC_000022.10:g.50307648_50307654dup , CM000684.1:g.50307648_50307654dup	GRCh37
NC_000022.9:g.48693652_48693658dup	NCBI36
NG_008927.1:g.9454_9460dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330817.11:c.-78-162_-78-156dup MANE Select	ENSP00000333813.5:n.-78-162_-78-156dup
ENST00000330817.10:c.-78-162_-78-156dup	ENSP00000333813.5:n.-78-162_-78-156dup
NM_024105.3:c.-78-162_-78-156dup	NP_077010.1:n.-78-162_-78-156dup
XM_011530369.1:c.-78-162_-78-156dup	XP_011528671.1:n.-78-162_-78-156dup
XM_011530370.1:c.-78-162_-78-156dup	XP_011528672.1:n.-78-162_-78-156dup
XM_011530371.1:c.-78-162_-78-156dup	XP_011528673.1:n.-78-162_-78-156dup
XM_011530371.2:c.-78-162_-78-156dup	XP_011528673.1:n.-78-162_-78-156dup
XM_017028936.1:c.-78-162_-78-156dup	XP_016884425.1:n.-78-162_-78-156dup
XM_017028937.1:c.-78-162_-78-156dup	XP_016884426.1:n.-78-162_-78-156dup
NM_024105.4:c.-78-162_-78-156dup MANE Select	NP_077010.1:n.-78-162_-78-156dup