Canonical Allele Identifier: CA376515737

Gene: PCDH15

Linked Data

• MyVariant Identifiers: chr10:g.55566371T>A (hg19) ; chr10:g.53806611T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.53806611T>A , CM000672.2:g.53806611T>A	GRCh38
NC_000010.10:g.55566371T>A , CM000672.1:g.55566371T>A	GRCh37
NC_000010.9:g.55236377T>A	NCBI36
NG_009191.2:g.999681A>T
NG_009191.3:g.1827572A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642496.1:c.4050A>T
ENST00000644397.2:c.5191A>T MANE Select	ENSP00000495195.1:p.Asn1731Tyr
ENST00000373965.6:c.5002A>T	ENSP00000363076.3:p.Asn1668Tyr
ENST00000414778.5:c.4999A>T	ENSP00000410304.2:p.Asn1667Tyr
ENST00000495484.5:c.1219A>T	ENSP00000480780.1:p.Asn407Tyr
ENST00000614895.4:c.5014A>T	ENSP00000478512.1:p.Asn1672Tyr
ENST00000616114.4:c.4996A>T	ENSP00000483745.1:p.Asn1666Tyr
ENST00000618301.4:c.1351A>T	ENSP00000482780.1:p.Asn451Tyr
ENST00000621708.4:c.5017A>T	ENSP00000484454.1:p.Asn1673Tyr
NM_001142771.1:c.5017A>T	NP_001136243.1:p.Asn1673Tyr
NM_001142772.1:c.5002A>T	NP_001136244.1:p.Asn1668Tyr
NM_001354420.1:c.4996A>T	NP_001341349.1:p.Asn1666Tyr
NM_001354429.1:c.5125A>T	NP_001341358.1:p.Asn1709Tyr
XR_001747192.2:n.11483A>T
XR_001747193.2:n.11474A>T
NM_001142771.2:c.5017A>T	NP_001136243.1:p.Asn1673Tyr
NM_001142772.2:c.5002A>T	NP_001136244.1:p.Asn1668Tyr
NM_001354420.2:c.4996A>T	NP_001341349.1:p.Asn1666Tyr
NM_001354429.2:c.5125A>T	NP_001341358.1:p.Asn1709Tyr
NM_001384140.1:c.5191A>T MANE Select	NP_001371069.1:p.Asn1731Tyr