Canonical Allele Identifier: CA372881920

Gene: GLDC

Linked Data

• MyVariant Identifiers: chr9:g.6558617A>T (hg19) ; chr9:g.6558617A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6558617A>T , CM000671.2:g.6558617A>T	GRCh38
NC_000009.11:g.6558617A>T , CM000671.1:g.6558617A>T	GRCh37
NC_000009.10:g.6548617A>T	NCBI36
NG_016397.1:g.92076T>A , LRG_643:g.92076T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.1994T>A MANE Select	ENSP00000370737.4:p.Ile665Asn
ENST00000460457.2:n.154T>A
ENST00000638233.1:n.429T>A
ENST00000638661.1:c.194T>A	ENSP00000491369.1:p.Ile65Asn
ENST00000638694.1:n.181T>A
ENST00000639318.1:c.194T>A	ENSP00000491932.1:p.Ile65Asn
ENST00000639364.1:n.1694T>A
ENST00000639443.1:n.1562T>A
ENST00000639954.1:n.1702T>A
ENST00000640208.1:c.194T>A	ENSP00000491895.1:p.Ile65Asn
ENST00000640505.1:n.233T>A
ENST00000640592.1:n.1877T>A
ENST00000321612.6:c.1994T>A	ENSP00000370737.3:p.Ile665Asn
ENST00000460457.1:n.133T>A
NM_000170.2:c.1994T>A , LRG_643t1:c.1994T>A	NP_000161.2:p.Ile665Asn
NM_000170.3:c.1994T>A MANE Select	NP_000161.2:p.Ile665Asn