Canonical Allele Identifier: CA337511129

Gene: PCDH11Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.5499864A>G , CM000686.2:g.5499864A>G	GRCh38
NC_000024.9:g.5367905A>G , CM000686.1:g.5367905A>G	GRCh37
NC_000024.8:g.5427905A>G	NCBI36
NG_011652.1:g.504639A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698851.1:c.2854-1193A>G MANE Select	ENSP00000513983.1:n.2854-1193A>G
ENST00000400457.3:c.3130-1193A>G	ENSP00000383306.3:n.3130-1193A>G
NM_032973.2:c.3130-1193A>G	NP_116755.1:n.3130-1193A>G
XM_011531476.1:c.3097-1193A>G	XP_011529778.1:n.3097-1193A>G
XM_011531477.1:c.3097-1193A>G	XP_011529779.1:n.3097-1193A>G
XM_011531478.1:c.2854-1193A>G	XP_011529780.1:n.2854-1193A>G
XM_017030079.1:c.3097-1193A>G	XP_016885568.1:n.3097-1193A>G
XM_017030080.1:c.3097-1193A>G	XP_016885569.1:n.3097-1193A>G
XM_017030081.1:c.3097-1193A>G	XP_016885570.1:n.3097-1193A>G
NM_001395587.1:c.2854-1193A>G MANE Select	NP_001382516.1:n.2854-1193A>G