Canonical Allele Identifier: CA1830493013

Gene: GLDC

Linked Data

• dbSNP Id: rs1817619173

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555934_6555937dup , CM000671.2:g.6555934_6555937dup	GRCh38
NC_000009.11:g.6555934_6555937dup , CM000671.1:g.6555934_6555937dup	GRCh37
NC_000009.10:g.6545934_6545937dup	NCBI36
NG_016397.1:g.94757_94760dup , LRG_643:g.94757_94760dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+217_2202+220dup MANE Select	ENSP00000370737.4:n.2202+217_2202+220dup
ENST00000638233.1:n.637+217_637+220dup
ENST00000638661.1:c.402+217_402+220dup	ENSP00000491369.1:n.402+217_402+220dup
ENST00000638694.1:n.389+217_389+220dup
ENST00000639318.1:c.402+217_402+220dup	ENSP00000491932.1:n.402+217_402+220dup
ENST00000639364.1:n.1902+217_1902+220dup
ENST00000639443.1:n.1770+217_1770+220dup
ENST00000639954.1:n.1910+217_1910+220dup
ENST00000640505.1:n.441+217_441+220dup
ENST00000321612.6:c.2202+217_2202+220dup	ENSP00000370737.3:n.2202+217_2202+220dup
NM_000170.2:c.2202+217_2202+220dup , LRG_643t1:c.2202+217_2202+220dup	NP_000161.2:n.2202+217_2202+220dup
NM_000170.3:c.2202+217_2202+220dup MANE Select	NP_000161.2:n.2202+217_2202+220dup