Canonical Allele Identifier: CA376516013

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566456A>C (hg19) ; chr10:g.53806696A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806696A>C , CM000672.2:g.53806696A>C	GRCh38
NC_000010.10:g.55566456A>C , CM000672.1:g.55566456A>C	GRCh37
NC_000010.9:g.55236462A>C	NCBI36
NG_009191.2:g.999596T>G
NG_009191.3:g.1827487T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3965T>G
ENST00000644397.2:c.5106T>G MANE Select	ENSP00000495195.1:p.Ile1702Met
ENST00000373965.6:c.4917T>G	ENSP00000363076.3:p.Ile1639Met
ENST00000414778.5:c.4914T>G	ENSP00000410304.2:p.Ile1638Met
ENST00000495484.5:c.1134T>G	ENSP00000480780.1:p.Ile378Met
ENST00000614895.4:c.4929T>G	ENSP00000478512.1:p.Ile1643Met
ENST00000616114.4:c.4911T>G	ENSP00000483745.1:p.Ile1637Met
ENST00000618301.4:c.1266T>G	ENSP00000482780.1:p.Ile422Met
ENST00000621708.4:c.4932T>G	ENSP00000484454.1:p.Ile1644Met
NM_001142771.1:c.4932T>G	NP_001136243.1:p.Ile1644Met
NM_001142772.1:c.4917T>G	NP_001136244.1:p.Ile1639Met
NM_001354420.1:c.4911T>G	NP_001341349.1:p.Ile1637Met
NM_001354429.1:c.5040T>G	NP_001341358.1:p.Ile1680Met
XR_001747192.2:n.11398T>G
XR_001747193.2:n.11389T>G
NM_001142771.2:c.4932T>G	NP_001136243.1:p.Ile1644Met
NM_001142772.2:c.4917T>G	NP_001136244.1:p.Ile1639Met
NM_001354420.2:c.4911T>G	NP_001341349.1:p.Ile1637Met
NM_001354429.2:c.5040T>G	NP_001341358.1:p.Ile1680Met
NM_001384140.1:c.5106T>G MANE Select	NP_001371069.1:p.Ile1702Met