Canonical Allele Identifier: CA1213317714
Gene: PLA2G4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186839211G>C , CM000663.2:g.186839211G>C GRCh38
NC_000001.10:g.186808343G>C , CM000663.1:g.186808343G>C GRCh37
NC_000001.9:g.185074966G>C NCBI36
NG_012203.1:g.15312G>C
NG_012203.2:g.15312G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367466.4:c.-70+10176G>C MANE Select ENSP00000356436.3:n.-70+10176G>C
ENST00000367466.3:c.-70+10176G>C ENSP00000356436.3:n.-70+10176G>C
NM_001311193.1:c.-70+10176G>C NP_001298122.1:n.-70+10176G>C
NM_024420.2:c.-70+10176G>C NP_077734.1:n.-70+10176G>C
XM_011509642.1:c.-70+10161G>C XP_011507944.1:n.-70+10161G>C
XM_011509642.2:c.-70+10161G>C XP_011507944.1:n.-70+10161G>C
NM_001311193.2:c.-70+10176G>C NP_001298122.2:n.-70+10176G>C
NM_024420.3:c.-70+10176G>C MANE Select NP_077734.2:n.-70+10176G>C