Canonical Allele Identifier: CA469545857

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566468C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806708C>T , CM000672.2:g.53806708C>T	GRCh38
NC_000010.10:g.55566468C>T , CM000672.1:g.55566468C>T	GRCh37
NC_000010.9:g.55236474C>T	NCBI36
NG_009191.2:g.999584G>A
NG_009191.3:g.1827475G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.3953G>A
ENST00000644397.2:c.5094G>A MANE Select	ENSP00000495195.1:p.Gln1698=
ENST00000373965.6:c.4905G>A	ENSP00000363076.3:p.Gln1635=
ENST00000414778.5:c.4902G>A	ENSP00000410304.2:p.Gln1634=
ENST00000495484.5:c.1122G>A	ENSP00000480780.1:p.Gln374=
ENST00000614895.4:c.4917G>A	ENSP00000478512.1:p.Gln1639=
ENST00000616114.4:c.4899G>A	ENSP00000483745.1:p.Gln1633=
ENST00000618301.4:c.1254G>A	ENSP00000482780.1:p.Gln418=
ENST00000621708.4:c.4920G>A	ENSP00000484454.1:p.Gln1640=
NM_001142771.1:c.4920G>A	NP_001136243.1:p.Gln1640=
NM_001142772.1:c.4905G>A	NP_001136244.1:p.Gln1635=
NM_001354420.1:c.4899G>A	NP_001341349.1:p.Gln1633=
NM_001354429.1:c.5028G>A	NP_001341358.1:p.Gln1676=
XR_001747192.2:n.11386G>A
XR_001747193.2:n.11377G>A
NM_001142771.2:c.4920G>A	NP_001136243.1:p.Gln1640=
NM_001142772.2:c.4905G>A	NP_001136244.1:p.Gln1635=
NM_001354420.2:c.4899G>A	NP_001341349.1:p.Gln1633=
NM_001354429.2:c.5028G>A	NP_001341358.1:p.Gln1676=
NM_001384140.1:c.5094G>A MANE Select	NP_001371069.1:p.Gln1698=