Canonical Allele Identifier: CA10496823

Gene: PLS3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.115610944C>A , CM000685.2:g.115610944C>A	GRCh38
NC_000023.10:g.114845256C>A , CM000685.1:g.114845256C>A	GRCh37
NC_000023.9:g.114751512C>A	NCBI36
NG_012518.2:g.55066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355899.8:c.73+621C>A MANE Select	ENSP00000348163.3:n.73+621C>A
ENST00000289290.7:c.7+23C>A	ENSP00000289290.4:n.7+23C>A
ENST00000355899.7:c.73+621C>A	ENSP00000348163.3:n.73+621C>A
ENST00000473026.6:c.73+621C>A	ENSP00000475900.1:n.73+621C>A
ENST00000481823.5:c.73+621C>A	ENSP00000419051.1:n.73+621C>A
ENST00000489283.5:c.73+621C>A	ENSP00000420458.1:n.73+621C>A
ENST00000539310.5:c.73+621C>A	ENSP00000445339.2:n.73+621C>A
ENST00000626746.2:c.73+621C>A	ENSP00000487343.1:n.73+621C>A
NM_001136025.4:c.73+621C>A	NP_001129497.1:n.73+621C>A
NM_001172335.2:c.73+621C>A	NP_001165806.1:n.73+621C>A
NM_001282337.1:c.7+23C>A	NP_001269266.1:n.7+23C>A
NM_001282338.1:c.-445+621C>A	NP_001269267.1:n.-445+621C>A
NM_005032.6:c.73+621C>A	NP_005023.2:n.73+621C>A
XM_011537534.1:c.73+621C>A	XP_011535836.1:n.73+621C>A
NM_005032.7:c.73+621C>A MANE Select	NP_005023.2:n.73+621C>A
NM_001136025.5:c.73+621C>A	NP_001129497.1:n.73+621C>A
NM_001172335.3:c.73+621C>A	NP_001165806.1:n.73+621C>A
NM_001282337.2:c.7+23C>A	NP_001269266.1:n.7+23C>A
NM_001282338.2:c.-445+621C>A	NP_001269267.1:n.-445+621C>A