Canonical Allele Identifier: CA2664894316
Community Standard Title: NM_015141.4(GPD1L):c.-51T>C
Gene: GPD1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32106661T>C , CM000665.2:g.32106661T>C GRCh38
NC_000003.11:g.32148153T>C , CM000665.1:g.32148153T>C GRCh37
NC_000003.10:g.32123157T>C NCBI36
NG_023375.1:g.5151T>C , LRG_419:g.5151T>C

Transcript Alleles

HGVS Amino-acid Change
NM_015141.4:c.-51T>C MANE Select NP_055956.1:n.-51T>C
ENST00000282541.10:c.-51T>C MANE Select ENSP00000282541.6:n.-51T>C
NM_015141.3:c.-51T>C , LRG_419t1:c.-51T>C NP_055956.1:n.-51T>C
ENST00000282541.9:c.-51T>C ENSP00000282541.5:n.-51T>C
ENST00000425459.5:c.-51T>C ENSP00000408770.1:n.-51T>C
ENST00000428684.1:c.-51T>C ENSP00000392199.1:n.-51T>C
ENST00000429432.5:c.-71+832T>C ENSP00000393861.1:n.-71+832T>C
XM_005264983.2:c.-51T>C XP_005265040.1:n.-51T>C
XM_006713068.2:c.-51T>C XP_006713131.1:n.-51T>C