Canonical Allele Identifier: CA918403269

Gene: GLDC

Linked Data

• dbSNP Id: rs1587924540

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555893_6555895del , CM000671.2:g.6555893_6555895del	GRCh38
NC_000009.11:g.6555893_6555895del , CM000671.1:g.6555893_6555895del	GRCh37
NC_000009.10:g.6545893_6545895del	NCBI36
NG_016397.1:g.94801_94803del , LRG_643:g.94801_94803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+261_2202+263del MANE Select	ENSP00000370737.4:n.2202+261_2202+263del
ENST00000638233.1:n.637+261_637+263del
ENST00000638661.1:c.402+261_402+263del	ENSP00000491369.1:n.402+261_402+263del
ENST00000638694.1:n.389+261_389+263del
ENST00000639318.1:c.402+261_402+263del	ENSP00000491932.1:n.402+261_402+263del
ENST00000639364.1:n.1902+261_1902+263del
ENST00000639443.1:n.1770+261_1770+263del
ENST00000639954.1:n.1910+261_1910+263del
ENST00000640505.1:n.441+261_441+263del
ENST00000321612.6:c.2202+261_2202+263del	ENSP00000370737.3:n.2202+261_2202+263del
NM_000170.2:c.2202+261_2202+263del , LRG_643t1:c.2202+261_2202+263del	NP_000161.2:n.2202+261_2202+263del
NM_000170.3:c.2202+261_2202+263del MANE Select	NP_000161.2:n.2202+261_2202+263del