Canonical Allele Identifier: CA334696697

Gene: PLS3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.115610501del , CM000685.2:g.115610501del	GRCh38
NC_000023.10:g.114844813del , CM000685.1:g.114844813del	GRCh37
NC_000023.9:g.114751069del	NCBI36
NG_012518.2:g.54623del

Transcript Alleles

HGVS	Amino-acid Change
NM_005032.7:c.73+178del MANE Select	NP_005023.2:n.73+178del
ENST00000355899.8:c.73+178del MANE Select	ENSP00000348163.3:n.73+178del
NM_001136025.4:c.73+178del	NP_001129497.1:n.73+178del
NM_001136025.5:c.73+178del	NP_001129497.1:n.73+178del
NM_001172335.2:c.73+178del	NP_001165806.1:n.73+178del
NM_001172335.3:c.73+178del	NP_001165806.1:n.73+178del
NM_001282337.1:c.-113+178del	NP_001269266.1:n.-113+178del
NM_001282337.2:c.-113+178del	NP_001269266.1:n.-113+178del
NM_001282338.1:c.-445+178del	NP_001269267.1:n.-445+178del
NM_001282338.2:c.-445+178del	NP_001269267.1:n.-445+178del
NM_005032.6:c.73+178del	NP_005023.2:n.73+178del
ENST00000289290.7:c.-113+178del	ENSP00000289290.4:n.-113+178del
ENST00000355899.7:c.73+178del	ENSP00000348163.3:n.73+178del
ENST00000473026.6:c.73+178del	ENSP00000475900.1:n.73+178del
ENST00000481823.5:c.73+178del	ENSP00000419051.1:n.73+178del
ENST00000489283.5:c.73+178del	ENSP00000420458.1:n.73+178del
ENST00000539310.5:c.73+178del	ENSP00000445339.2:n.73+178del
ENST00000626746.2:c.73+178del	ENSP00000487343.1:n.73+178del
XM_011537534.1:c.73+178del	XP_011535836.1:n.73+178del