Canonical Allele Identifier: CA4980337
Community Standard Title: NM_000170.3(GLDC):c.2203-19G>A
Gene: GLDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6554800C>T , CM000671.2:g.6554800C>T GRCh38
NC_000009.11:g.6554800C>T , CM000671.1:g.6554800C>T GRCh37
NC_000009.10:g.6544800C>T NCBI36
NG_016397.1:g.95893G>A , LRG_643:g.95893G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000170.3:c.2203-19G>A MANE Select NP_000161.2:n.2203-19G>A
ENST00000321612.8:c.2203-19G>A MANE Select ENSP00000370737.4:n.2203-19G>A
NM_000170.2:c.2203-19G>A , LRG_643t1:c.2203-19G>A NP_000161.2:n.2203-19G>A
ENST00000321612.6:c.2203-19G>A ENSP00000370737.3:n.2203-19G>A
ENST00000467946.1:n.110G>A
ENST00000638233.1:n.638-19G>A
ENST00000638661.1:c.403-19G>A ENSP00000491369.1:n.403-19G>A
ENST00000638694.1:n.390-19G>A
ENST00000639318.1:c.403-19G>A ENSP00000491932.1:n.403-19G>A
ENST00000639364.1:n.1903-19G>A
ENST00000639443.1:n.1771-19G>A
ENST00000639639.1:c.-115G>A ENSP00000491312.1:n.-115G>A
ENST00000639954.1:n.1911-19G>A
ENST00000640505.1:n.442-19G>A