Canonical Allele Identifier: CA2296651
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32140328A>G , CM000665.2:g.32140328A>G GRCh38
NC_000003.11:g.32181820A>G , CM000665.1:g.32181820A>G GRCh37
NC_000003.10:g.32156824A>G NCBI36
NG_023375.1:g.38818A>G , LRG_419:g.38818A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282541.10:c.467A>G MANE Select ENSP00000282541.6:p.Asn156Ser
ENST00000282541.9:c.467A>G ENSP00000282541.5:p.Asn156Ser
ENST00000425459.5:c.326A>G ENSP00000408770.1:p.Asn109Ser
ENST00000428684.1:c.*94A>G ENSP00000392199.1:n.*94A>G
ENST00000429432.5:c.350A>G ENSP00000393861.1:p.Asn117Ser
ENST00000431009.1:c.350A>G ENSP00000416518.1:p.Asn117Ser
NM_015141.3:c.467A>G , LRG_419t1:c.467A>G NP_055956.1:p.Asn156Ser
XM_005264983.2:c.467A>G XP_005265040.1:p.Asn156Ser
XM_006713068.2:c.326A>G XP_006713131.1:p.Asn109Ser
NM_015141.4:c.467A>G MANE Select NP_055956.1:p.Asn156Ser