Canonical Allele Identifier: CA432928592
Community Standard Title: NM_015141.4(GPD1L):c.216A>T (p.Pro72=)
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32128244A>T , CM000665.2:g.32128244A>T GRCh38
NC_000003.11:g.32169736A>T , CM000665.1:g.32169736A>T GRCh37
NC_000003.10:g.32144740A>T NCBI36
NG_023375.1:g.26734A>T , LRG_419:g.26734A>T

Transcript Alleles

HGVS Amino-acid Change
NM_015141.4:c.216A>T MANE Select NP_055956.1:p.Pro72=
ENST00000282541.10:c.216A>T MANE Select ENSP00000282541.6:p.Pro72=
NM_015141.3:c.216A>T , LRG_419t1:c.216A>T NP_055956.1:p.Pro72=
ENST00000282541.9:c.216A>T ENSP00000282541.5:p.Pro72=
ENST00000425459.5:c.216A>T ENSP00000408770.1:p.Pro72=
ENST00000428684.1:c.48-10343A>T ENSP00000392199.1:n.48-10343A>T
ENST00000429432.5:c.99A>T ENSP00000393861.1:p.Pro33=
ENST00000431009.1:c.99A>T ENSP00000416518.1:p.Pro33=
XM_005264983.2:c.216A>T XP_005265040.1:p.Pro72=
XM_006713068.2:c.216A>T XP_006713131.1:p.Pro72=