Canonical Allele Identifier: CA463584837

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6554776T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6554776T>G , CM000671.2:g.6554776T>G	GRCh38
NC_000009.11:g.6554776T>G , CM000671.1:g.6554776T>G	GRCh37
NC_000009.10:g.6544776T>G	NCBI36
NG_016397.1:g.95917A>C , LRG_643:g.95917A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321612.8:c.2208A>C MANE Select	ENSP00000370737.4:p.Gly736=
ENST00000638233.1:n.643A>C
ENST00000638661.1:c.408A>C	ENSP00000491369.1:p.Gly136=
ENST00000638694.1:n.395A>C
ENST00000639318.1:c.408A>C	ENSP00000491932.1:p.Gly136=
ENST00000639364.1:n.1908A>C
ENST00000639443.1:n.1776A>C
ENST00000639639.1:c.-91A>C	ENSP00000491312.1:n.-91A>C
ENST00000639954.1:n.1916A>C
ENST00000640505.1:n.447A>C
ENST00000321612.6:c.2208A>C	ENSP00000370737.3:p.Gly736=
ENST00000467946.1:n.134A>C
NM_000170.2:c.2208A>C , LRG_643t1:c.2208A>C	NP_000161.2:p.Gly736=
NM_000170.3:c.2208A>C MANE Select	NP_000161.2:p.Gly736=