Canonical Allele Identifier: CA432930610
Community Standard Title: NM_015141.4(GPD1L):c.288C>G (p.Pro96=)
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32138649C>G , CM000665.2:g.32138649C>G GRCh38
NC_000003.11:g.32180141C>G , CM000665.1:g.32180141C>G GRCh37
NC_000003.10:g.32155145C>G NCBI36
NG_023375.1:g.37139C>G , LRG_419:g.37139C>G

Transcript Alleles

HGVS Amino-acid Change
NM_015141.4:c.288C>G MANE Select NP_055956.1:p.Pro96=
ENST00000282541.10:c.288C>G MANE Select ENSP00000282541.6:p.Pro96=
NM_015141.3:c.288C>G , LRG_419t1:c.288C>G NP_055956.1:p.Pro96=
ENST00000282541.9:c.288C>G ENSP00000282541.5:p.Pro96=
ENST00000425459.5:c.226-1579C>G ENSP00000408770.1:n.226-1579C>G
ENST00000428684.1:c.110C>G ENSP00000392199.1:p.Pro37Arg
ENST00000429432.5:c.171C>G ENSP00000393861.1:p.Pro57=
ENST00000431009.1:c.171C>G ENSP00000416518.1:p.Pro57=
XM_005264983.2:c.288C>G XP_005265040.1:p.Pro96=
XM_006713068.2:c.226-1579C>G XP_006713131.1:n.226-1579C>G