Canonical Allele Identifier: CA2840286331

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784953dup , CM000672.2:g.71784953dup	GRCh38
NC_000010.10:g.73544710dup , CM000672.1:g.73544710dup	GRCh37
NC_000010.9:g.73214716dup	NCBI36
NG_008835.1:g.393007dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5565dup MANE Select	ENSP00000224721.9:p.Met1856HisfsTer22
ENST00000224721.10:c.5580dup	ENSP00000224721.8:p.Met1861HisfsTer22
ENST00000622827.4:c.5565dup	ENSP00000483211.1:p.Met1856HisfsTer22
NM_022124.5:c.5565dup	NP_071407.4:p.Met1856HisfsTer22
XM_006717940.2:c.5760dup	XP_006718003.1:p.Met1921HisfsTer22
XM_006717942.2:c.5694dup	XP_006718005.1:p.Met1899HisfsTer22
XM_011540039.1:c.5757dup	XP_011538341.1:p.Met1920HisfsTer22
XM_011540040.1:c.5754dup	XP_011538342.1:p.Met1919HisfsTer22
XM_011540041.1:c.5700dup	XP_011538343.1:p.Met1901HisfsTer22
XM_011540042.1:c.5760dup	XP_011538344.1:p.Met1921HisfsTer22
XM_011540043.1:c.5760dup	XP_011538345.1:p.Met1921HisfsTer22
XM_011540044.1:c.5625dup	XP_011538346.1:p.Met1876HisfsTer22
XM_011540045.1:c.5760dup	XP_011538347.1:p.Met1921HisfsTer22
XM_011540046.1:c.5220dup	XP_011538348.1:p.Met1741HisfsTer22
XM_011540047.1:c.4578dup	XP_011538349.1:p.Met1527HisfsTer22
XM_011540048.1:c.5760dup	XP_011538350.1:p.Met1921HisfsTer22
XM_011540049.1:c.5760dup	XP_011538351.1:p.Met1921HisfsTer22
XM_011540050.1:c.5760dup	XP_011538352.1:p.Met1921HisfsTer22
XM_011540051.1:c.5760dup	XP_011538353.1:p.Met1921HisfsTer22
XM_011540052.1:c.2088dup	XP_011538354.1:p.Met697HisfsTer22
XM_011540053.1:c.5760dup	XP_011538355.1:p.Met1921HisfsTer22
XR_945796.1:n.6003dup
NM_022124.6:c.5565dup MANE Select	NP_071407.4:p.Met1856HisfsTer22