Canonical Allele Identifier: CA376516516

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566570C>G (hg19) ; chr10:g.53806810C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806810C>G , CM000672.2:g.53806810C>G	GRCh38
NC_000010.10:g.55566570C>G , CM000672.1:g.55566570C>G	GRCh37
NC_000010.9:g.55236576C>G	NCBI36
NG_009191.2:g.999482G>C
NG_009191.3:g.1827373G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642496.1:c.3851G>C
ENST00000644397.2:c.4992G>C MANE Select	ENSP00000495195.1:p.Met1664Ile
ENST00000373965.6:c.4803G>C	ENSP00000363076.3:p.Met1601Ile
ENST00000414778.5:c.4800G>C	ENSP00000410304.2:p.Met1600Ile
ENST00000495484.5:c.1020G>C	ENSP00000480780.1:p.Met340Ile
ENST00000614895.4:c.4815G>C	ENSP00000478512.1:p.Met1605Ile
ENST00000616114.4:c.4797G>C	ENSP00000483745.1:p.Met1599Ile
ENST00000618301.4:c.1152G>C	ENSP00000482780.1:p.Met384Ile
ENST00000621708.4:c.4818G>C	ENSP00000484454.1:p.Met1606Ile
NM_001142771.1:c.4818G>C	NP_001136243.1:p.Met1606Ile
NM_001142772.1:c.4803G>C	NP_001136244.1:p.Met1601Ile
NM_001354420.1:c.4797G>C	NP_001341349.1:p.Met1599Ile
NM_001354429.1:c.4926G>C	NP_001341358.1:p.Met1642Ile
XR_001747192.2:n.11284G>C
XR_001747193.2:n.11275G>C
NM_001142771.2:c.4818G>C	NP_001136243.1:p.Met1606Ile
NM_001142772.2:c.4803G>C	NP_001136244.1:p.Met1601Ile
NM_001354420.2:c.4797G>C	NP_001341349.1:p.Met1599Ile
NM_001354429.2:c.4926G>C	NP_001341358.1:p.Met1642Ile
NM_001384140.1:c.4992G>C MANE Select	NP_001371069.1:p.Met1664Ile