Canonical Allele Identifier: CA1830491483
Community Standard Title: NM_000170.3(GLDC):c.2258A= (p.His753=)
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6554726T= , CM000671.2:g.6554726T= GRCh38
NC_000009.11:g.6554726T= , CM000671.1:g.6554726T= GRCh37
NC_000009.10:g.6544726T= NCBI36
NG_016397.1:g.95967A= , LRG_643:g.95967A=

Transcript Alleles

HGVS Amino-acid Change
NM_000170.3:c.2258A= MANE Select NP_000161.2:p.His753=
ENST00000321612.8:c.2258A= MANE Select ENSP00000370737.4:p.His753=
NM_000170.2:c.2258A= , LRG_643t1:c.2258A= NP_000161.2:p.His753=
ENST00000321612.6:c.2258A= ENSP00000370737.3:p.His753=
ENST00000467946.1:n.184A=
ENST00000638233.1:n.693A=
ENST00000638661.1:c.458A= ENSP00000491369.1:p.His153=
ENST00000638694.1:n.445A=
ENST00000639318.1:c.458A= ENSP00000491932.1:p.His153=
ENST00000639364.1:n.1958A=
ENST00000639443.1:n.1826A=
ENST00000639639.1:c.-41A= ENSP00000491312.1:n.-41A=
ENST00000639954.1:n.1966A=
ENST00000640505.1:n.497A=