Canonical Allele Identifier: CA1830492813

Gene: GLDC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6555794_6555798delinsAAAAG , CM000671.2:g.6555794_6555798delinsAAAAG	GRCh38
NC_000009.11:g.6555794_6555798delinsAAAAG , CM000671.1:g.6555794_6555798delinsAAAAG	GRCh37
NC_000009.10:g.6545794_6545798delinsAAAAG	NCBI36
NG_016397.1:g.94895_94899delinsCTTTT , LRG_643:g.94895_94899delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2202+355_2202+359delinsCTTTT MANE Select	ENSP00000370737.4:n.2202+355_2202+359delinsCTTTT
ENST00000638233.1:n.637+355_637+359delinsCTTTT
ENST00000638661.1:c.402+355_402+359delinsCTTTT	ENSP00000491369.1:n.402+355_402+359delinsCTTTT
ENST00000638694.1:n.389+355_389+359delinsCTTTT
ENST00000639318.1:c.402+355_402+359delinsCTTTT	ENSP00000491932.1:n.402+355_402+359delinsCTTTT
ENST00000639364.1:n.1902+355_1902+359delinsCTTTT
ENST00000639443.1:n.1770+355_1770+359delinsCTTTT
ENST00000639954.1:n.1910+355_1910+359delinsCTTTT
ENST00000640505.1:n.441+355_441+359delinsCTTTT
ENST00000321612.6:c.2202+355_2202+359delinsCTTTT	ENSP00000370737.3:n.2202+355_2202+359delinsCTTTT
NM_000170.2:c.2202+355_2202+359delinsCTTTT , LRG_643t1:c.2202+355_2202+359delinsCTTTT	NP_000161.2:n.2202+355_2202+359delinsCTTTT
NM_000170.3:c.2202+355_2202+359delinsCTTTT MANE Select	NP_000161.2:n.2202+355_2202+359delinsCTTTT