Canonical Allele Identifier: CA585762630

Gene: GLDC

Linked Data

• dbSNP Id: rs1243701357
• gnomAD v2: 9-6555932-TA-T
• gnomAD v3: 9-6555932-TA-T
• gnomAD v4: 9-6555932-TA-T
• MyVariant Identifiers: chr9:g.6555933del (hg19) ; chr9:g.6555933del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555934del , CM000671.2:g.6555934del	GRCh38
NC_000009.11:g.6555934del , CM000671.1:g.6555934del	GRCh37
NC_000009.10:g.6545934del	NCBI36
NG_016397.1:g.94760del , LRG_643:g.94760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+220del MANE Select	ENSP00000370737.4:n.2202+220del
ENST00000638233.1:n.637+220del
ENST00000638661.1:c.402+220del	ENSP00000491369.1:n.402+220del
ENST00000638694.1:n.389+220del
ENST00000639318.1:c.402+220del	ENSP00000491932.1:n.402+220del
ENST00000639364.1:n.1902+220del
ENST00000639443.1:n.1770+220del
ENST00000639954.1:n.1910+220del
ENST00000640505.1:n.441+220del
ENST00000321612.6:c.2202+220del	ENSP00000370737.3:n.2202+220del
NM_000170.2:c.2202+220del , LRG_643t1:c.2202+220del	NP_000161.2:n.2202+220del
NM_000170.3:c.2202+220del MANE Select	NP_000161.2:n.2202+220del