Canonical Allele Identifier: CA1157377478
Gene: PLA2G5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20082881A>T , CM000663.2:g.20082881A>T GRCh38
NC_000001.10:g.20409374A>T , CM000663.1:g.20409374A>T GRCh37
NC_000001.9:g.20281961A>T NCBI36
NG_032045.1:g.17674A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375108.4:c.-10-1940A>T MANE Select ENSP00000364249.3:n.-10-1940A>T
ENST00000375108.3:c.-10-1940A>T ENSP00000364249.3:n.-10-1940A>T
ENST00000460175.5:n.770-1940A>T
ENST00000465698.5:n.502-1940A>T
ENST00000469069.5:n.525-1940A>T
ENST00000478803.1:n.310-1940A>T
ENST00000486277.5:n.947-1940A>T
ENST00000489871.5:n.578-1940A>T
NM_000929.2:c.-10-1940A>T NP_000920.1:n.-10-1940A>T
XM_005245891.3:c.84-1940A>T XP_005245948.1:n.84-1940A>T
XM_005245892.3:c.84-1940A>T XP_005245949.1:n.84-1940A>T
XM_005245893.3:c.-10-1940A>T XP_005245950.1:n.-10-1940A>T
XM_006710696.2:c.-10-1940A>T XP_006710759.1:n.-10-1940A>T
XM_011541584.1:c.84-1940A>T XP_011539886.1:n.84-1940A>T
XM_011541585.1:c.84-1940A>T XP_011539887.1:n.84-1940A>T
XM_011541586.1:c.84-1940A>T XP_011539888.1:n.84-1940A>T
XM_011541587.1:c.-10-1940A>T XP_011539889.1:n.-10-1940A>T
XM_011541588.1:c.-10-1940A>T XP_011539890.1:n.-10-1940A>T
XM_011541589.1:c.-10-1940A>T XP_011539891.1:n.-10-1940A>T
XM_011541590.1:c.-10-1940A>T XP_011539892.1:n.-10-1940A>T
XM_011541591.1:c.-10-1940A>T XP_011539893.1:n.-10-1940A>T
XM_011541592.1:c.-10-1940A>T XP_011539894.1:n.-10-1940A>T
XM_005245891.5:c.84-1940A>T XP_005245948.1:n.84-1940A>T
XM_005245892.5:c.84-1940A>T XP_005245949.1:n.84-1940A>T
XM_005245893.5:c.-10-1940A>T XP_005245950.1:n.-10-1940A>T
XM_011541586.3:c.84-1940A>T XP_011539888.1:n.84-1940A>T
XM_011541587.3:c.-10-1940A>T XP_011539889.1:n.-10-1940A>T
XM_011541588.3:c.-10-1940A>T XP_011539890.1:n.-10-1940A>T
XM_011541589.3:c.-10-1940A>T XP_011539891.1:n.-10-1940A>T
XM_011541590.3:c.-10-1940A>T XP_011539892.1:n.-10-1940A>T
XM_011541591.3:c.-10-1940A>T XP_011539893.1:n.-10-1940A>T
XM_011541592.3:c.-10-1940A>T XP_011539894.1:n.-10-1940A>T
XM_024447706.1:c.-10-1940A>T XP_024303474.1:n.-10-1940A>T
NM_000929.3:c.-10-1940A>T MANE Select NP_000920.1:n.-10-1940A>T