Canonical Allele Identifier: CA337502138
Gene: PCDH11Y HGNC NCBI

Linked Data

dbSNP Id: rs4252209
gnomAD v3: Y-5057596-G-T
gnomAD v4: Y-5057596-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.5057596G>T , CM000686.2:g.5057596G>T GRCh38
NC_000024.9:g.4925637G>T , CM000686.1:g.4925637G>T GRCh37
NC_000024.8:g.4985637G>T NCBI36
NG_011652.1:g.62371G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698851.1:c.360+137G>T MANE Select ENSP00000513983.1:n.360+137G>T
ENST00000698927.1:c.603+137G>T ENSP00000514038.1:n.603+137G>T
ENST00000215473.7:c.636+137G>T ENSP00000215473.7:n.636+137G>T
ENST00000333703.8:c.603+137G>T ENSP00000330552.4:n.603+137G>T
ENST00000362095.9:c.636+137G>T ENSP00000355419.5:n.636+137G>T
ENST00000400457.3:c.636+137G>T ENSP00000383306.3:n.636+137G>T
ENST00000622698.4:c.603+137G>T ENSP00000482115.1:n.603+137G>T
NM_001278619.1:c.603+137G>T NP_001265548.1:n.603+137G>T
NM_032971.2:c.603+137G>T NP_116753.1:n.603+137G>T
NM_032972.2:c.636+137G>T NP_116754.1:n.636+137G>T
NM_032973.2:c.636+137G>T NP_116755.1:n.636+137G>T
XM_011531476.1:c.603+137G>T XP_011529778.1:n.603+137G>T
XM_011531477.1:c.603+137G>T XP_011529779.1:n.603+137G>T
XM_011531478.1:c.360+137G>T XP_011529780.1:n.360+137G>T
XM_017030079.1:c.603+137G>T XP_016885568.1:n.603+137G>T
XM_017030080.1:c.603+137G>T XP_016885569.1:n.603+137G>T
XM_017030081.1:c.603+137G>T XP_016885570.1:n.603+137G>T
XM_017030082.1:c.603+137G>T XP_016885571.1:n.603+137G>T
XM_017030083.1:c.360+137G>T XP_016885572.1:n.360+137G>T
NM_001278619.2:c.603+137G>T NP_001265548.1:n.603+137G>T
NM_032971.3:c.603+137G>T NP_116753.1:n.603+137G>T
NM_032972.3:c.636+137G>T NP_116754.1:n.636+137G>T
NM_001395587.1:c.360+137G>T MANE Select NP_001382516.1:n.360+137G>T