Canonical Allele Identifier: CA2609239

Gene: PLXND1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129585979G>A , CM000665.2:g.129585979G>A	GRCh38
NC_000003.11:g.129304822G>A , CM000665.1:g.129304822G>A	GRCh37
NC_000003.10:g.130787512G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015103.3:c.1824C>T MANE Select	NP_055918.3:p.Ser608=
ENST00000324093.9:c.1824C>T MANE Select	ENSP00000317128.4:p.Ser608=
NM_015103.2:c.1824C>T	NP_055918.2:p.Ser608=
ENST00000324093.8:c.1824C>T	ENSP00000317128.4:p.Ser608=
ENST00000505237.2:c.480C>T	ENSP00000426241.2:p.Ser160=
ENST00000505665.5:c.302C>T
XM_011512588.1:c.1824C>T	XP_011510890.1:p.Ser608=
XM_011512588.2:c.1824C>T	XP_011510890.1:p.Ser608=
XM_011512589.1:c.1824C>T	XP_011510891.1:p.Ser608=
XM_011512590.1:c.1824C>T	XP_011510892.1:p.Ser608=
XM_011512590.2:c.1824C>T	XP_011510892.1:p.Ser608=
XM_011512591.1:c.1824C>T	XP_011510893.1:p.Ser608=
XR_001740063.1:n.1839C>T
XR_924116.1:n.1839C>T