Canonical Allele Identifier: CA372881953

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558631C>T (hg19) ; chr9:g.6558631C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558631C>T , CM000671.2:g.6558631C>T	GRCh38
NC_000009.11:g.6558631C>T , CM000671.1:g.6558631C>T	GRCh37
NC_000009.10:g.6548631C>T	NCBI36
NG_016397.1:g.92062G>A , LRG_643:g.92062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1980G>A MANE Select	ENSP00000370737.4:p.Met660Ile
ENST00000460457.2:n.140G>A
ENST00000638233.1:n.415G>A
ENST00000638661.1:c.180G>A	ENSP00000491369.1:p.Met60Ile
ENST00000638694.1:n.167G>A
ENST00000639318.1:c.180G>A	ENSP00000491932.1:p.Met60Ile
ENST00000639364.1:n.1680G>A
ENST00000639443.1:n.1548G>A
ENST00000639954.1:n.1688G>A
ENST00000640208.1:c.180G>A	ENSP00000491895.1:p.Met60Ile
ENST00000640505.1:n.219G>A
ENST00000640592.1:n.1863G>A
ENST00000321612.6:c.1980G>A	ENSP00000370737.3:p.Met660Ile
ENST00000460457.1:n.119G>A
NM_000170.2:c.1980G>A , LRG_643t1:c.1980G>A	NP_000161.2:p.Met660Ile
NM_000170.3:c.1980G>A MANE Select	NP_000161.2:p.Met660Ile