Canonical Allele Identifier: CA377160914

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562809A>C (hg19) ; chr10:g.71803052A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803052A>C , CM000672.2:g.71803052A>C	GRCh38
NC_000010.10:g.73562809A>C , CM000672.1:g.73562809A>C	GRCh37
NC_000010.9:g.73232815A>C	NCBI36
NG_008835.1:g.411106A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7637A>C MANE Select	ENSP00000224721.9:p.Tyr2546Ser
ENST00000642965.1:c.1570A>C	ENSP00000495222.1:n.1570A>C
ENST00000647092.1:c.1234A>C	ENSP00000495176.1:n.1234A>C
ENST00000224721.10:c.7652A>C	ENSP00000224721.8:p.Tyr2551Ser
ENST00000398788.4:c.917A>C	ENSP00000381768.3:p.Tyr306Ser
ENST00000475158.1:n.1173A>C
ENST00000619887.4:c.917A>C	ENSP00000478374.1:p.Tyr306Ser
ENST00000622827.4:c.7637A>C	ENSP00000483211.1:p.Tyr2546Ser
NM_001171933.1:c.917A>C	NP_001165404.1:p.Tyr306Ser
NM_001171934.1:c.917A>C	NP_001165405.1:p.Tyr306Ser
NM_022124.5:c.7637A>C	NP_071407.4:p.Tyr2546Ser
XM_006717940.2:c.7832A>C	XP_006718003.1:p.Tyr2611Ser
XM_006717942.2:c.7766A>C	XP_006718005.1:p.Tyr2589Ser
XM_011540039.1:c.7829A>C	XP_011538341.1:p.Tyr2610Ser
XM_011540040.1:c.7826A>C	XP_011538342.1:p.Tyr2609Ser
XM_011540041.1:c.7772A>C	XP_011538343.1:p.Tyr2591Ser
XM_011540042.1:c.7742A>C	XP_011538344.1:p.Tyr2581Ser
XM_011540043.1:c.7832A>C	XP_011538345.1:p.Tyr2611Ser
XM_011540044.1:c.7697A>C	XP_011538346.1:p.Tyr2566Ser
XM_011540045.1:c.7832A>C	XP_011538347.1:p.Tyr2611Ser
XM_011540046.1:c.7292A>C	XP_011538348.1:p.Tyr2431Ser
XM_011540047.1:c.6650A>C	XP_011538349.1:p.Tyr2217Ser
XM_011540052.1:c.4160A>C	XP_011538354.1:p.Tyr1387Ser
NM_022124.6:c.7637A>C MANE Select	NP_071407.4:p.Tyr2546Ser