Canonical Allele Identifier: CA372881883

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558599T>G (hg19) ; chr9:g.6558599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558599T>G , CM000671.2:g.6558599T>G	GRCh38
NC_000009.11:g.6558599T>G , CM000671.1:g.6558599T>G	GRCh37
NC_000009.10:g.6548599T>G	NCBI36
NG_016397.1:g.92094A>C , LRG_643:g.92094A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2012A>C MANE Select	ENSP00000370737.4:p.Asp671Ala
ENST00000460457.2:n.172A>C
ENST00000638233.1:n.447A>C
ENST00000638661.1:c.212A>C	ENSP00000491369.1:p.Asp71Ala
ENST00000638694.1:n.199A>C
ENST00000639318.1:c.212A>C	ENSP00000491932.1:p.Asp71Ala
ENST00000639364.1:n.1712A>C
ENST00000639443.1:n.1580A>C
ENST00000639954.1:n.1720A>C
ENST00000640208.1:c.212A>C	ENSP00000491895.1:p.Asp71Ala
ENST00000640505.1:n.251A>C
ENST00000640592.1:n.1895A>C
ENST00000321612.6:c.2012A>C	ENSP00000370737.3:p.Asp671Ala
ENST00000460457.1:n.151A>C
NM_000170.2:c.2012A>C , LRG_643t1:c.2012A>C	NP_000161.2:p.Asp671Ala
NM_000170.3:c.2012A>C MANE Select	NP_000161.2:p.Asp671Ala