Canonical Allele Identifier: CA188651055

Gene: GLDC

Linked Data

• dbSNP Id: rs372279183
• MyVariant Identifiers: chr9:g.6556459_6556460insAAACC (hg19) ; chr9:g.6556459_6556460insAAACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6556459_6556460insAAACC , CM000671.2:g.6556459_6556460insAAACC	GRCh38
NC_000009.11:g.6556459_6556460insAAACC , CM000671.1:g.6556459_6556460insAAACC	GRCh37
NC_000009.10:g.6546459_6546460insAAACC	NCBI36
NG_016397.1:g.94233_94234insGGTTT , LRG_643:g.94233_94234insGGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321612.8:c.2053-158_2053-157insGGTTT MANE Select	ENSP00000370737.4:n.2053-158_2053-157insGGTTT
ENST00000638233.1:n.488-158_488-157insGGTTT
ENST00000638661.1:c.253-158_253-157insGGTTT	ENSP00000491369.1:n.253-158_253-157insGGTTT
ENST00000638694.1:n.240-158_240-157insGGTTT
ENST00000639318.1:c.253-158_253-157insGGTTT	ENSP00000491932.1:n.253-158_253-157insGGTTT
ENST00000639364.1:n.1753-158_1753-157insGGTTT
ENST00000639443.1:n.1621-158_1621-157insGGTTT
ENST00000639954.1:n.1761-158_1761-157insGGTTT
ENST00000640505.1:n.292-158_292-157insGGTTT
ENST00000321612.6:c.2053-158_2053-157insGGTTT	ENSP00000370737.3:n.2053-158_2053-157insGGTTT
NM_000170.2:c.2053-158_2053-157insGGTTT , LRG_643t1:c.2053-158_2053-157insGGTTT	NP_000161.2:n.2053-158_2053-157insGGTTT
NM_000170.3:c.2053-158_2053-157insGGTTT MANE Select	NP_000161.2:n.2053-158_2053-157insGGTTT