Canonical Allele Identifier: CA2296529
Community Standard Title: NM_015141.4(GPD1L):c.1A>G (p.Met1Val)
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32106712A>G , CM000665.2:g.32106712A>G GRCh38
NC_000003.11:g.32148204A>G , CM000665.1:g.32148204A>G GRCh37
NC_000003.10:g.32123208A>G NCBI36
NG_023375.1:g.5202A>G , LRG_419:g.5202A>G

Transcript Alleles

HGVS Amino-acid Change
NM_015141.4:c.1A>G MANE Select NP_055956.1:p.Met1Val
ENST00000282541.10:c.1A>G MANE Select ENSP00000282541.6:p.Met1Val
NM_015141.3:c.1A>G , LRG_419t1:c.1A>G NP_055956.1:p.Met1Val
ENST00000282541.9:c.1A>G ENSP00000282541.5:p.Met1Val
ENST00000425459.5:c.1A>G ENSP00000408770.1:p.Met1Val
ENST00000428684.1:c.1A>G ENSP00000392199.1:p.Met1Val
ENST00000429432.5:c.-71+883A>G ENSP00000393861.1:n.-71+883A>G
ENST00000431009.1:c.-176A>G ENSP00000416518.1:n.-176A>G
XM_005264983.2:c.1A>G XP_005265040.1:p.Met1Val
XM_006713068.2:c.1A>G XP_006713131.1:p.Met1Val