Canonical Allele Identifier: CA432928484
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32128154C>G , CM000665.2:g.32128154C>G GRCh38
NC_000003.11:g.32169646C>G , CM000665.1:g.32169646C>G GRCh37
NC_000003.10:g.32144650C>G NCBI36
NG_023375.1:g.26644C>G , LRG_419:g.26644C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282541.10:c.126C>G MANE Select ENSP00000282541.6:p.Val42=
ENST00000282541.9:c.126C>G ENSP00000282541.5:p.Val42=
ENST00000425459.5:c.126C>G ENSP00000408770.1:p.Val42=
ENST00000428684.1:c.48-10433C>G ENSP00000392199.1:n.48-10433C>G
ENST00000429432.5:c.9C>G ENSP00000393861.1:p.Val3=
ENST00000431009.1:c.9C>G ENSP00000416518.1:p.Val3=
NM_015141.3:c.126C>G , LRG_419t1:c.126C>G NP_055956.1:p.Val42=
XM_005264983.2:c.126C>G XP_005265040.1:p.Val42=
XM_006713068.2:c.126C>G XP_006713131.1:p.Val42=
NM_015141.4:c.126C>G MANE Select NP_055956.1:p.Val42=