Canonical Allele Identifier: CA377159402

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559319G>C (hg19) ; chr10:g.71799562G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799562G>C , CM000672.2:g.71799562G>C	GRCh38
NC_000010.10:g.73559319G>C , CM000672.1:g.73559319G>C	GRCh37
NC_000010.9:g.73229325G>C	NCBI36
NG_008835.1:g.407616G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7295G>C MANE Select	ENSP00000224721.9:p.Gly2432Ala
ENST00000642965.1:c.1228G>C	ENSP00000495222.1:n.1228G>C
ENST00000647092.1:c.892G>C	ENSP00000495176.1:n.892G>C
ENST00000224721.10:c.7310G>C	ENSP00000224721.8:p.Gly2437Ala
ENST00000398788.4:c.575G>C	ENSP00000381768.3:p.Gly192Ala
ENST00000475158.1:n.831G>C
ENST00000619887.4:c.575G>C	ENSP00000478374.1:p.Gly192Ala
ENST00000622827.4:c.7295G>C	ENSP00000483211.1:p.Gly2432Ala
NM_001171933.1:c.575G>C	NP_001165404.1:p.Gly192Ala
NM_001171934.1:c.575G>C	NP_001165405.1:p.Gly192Ala
NM_022124.5:c.7295G>C	NP_071407.4:p.Gly2432Ala
XM_006717940.2:c.7490G>C	XP_006718003.1:p.Gly2497Ala
XM_006717942.2:c.7424G>C	XP_006718005.1:p.Gly2475Ala
XM_011540039.1:c.7487G>C	XP_011538341.1:p.Gly2496Ala
XM_011540040.1:c.7484G>C	XP_011538342.1:p.Gly2495Ala
XM_011540041.1:c.7430G>C	XP_011538343.1:p.Gly2477Ala
XM_011540042.1:c.7400G>C	XP_011538344.1:p.Gly2467Ala
XM_011540043.1:c.7490G>C	XP_011538345.1:p.Gly2497Ala
XM_011540044.1:c.7355G>C	XP_011538346.1:p.Gly2452Ala
XM_011540045.1:c.7490G>C	XP_011538347.1:p.Gly2497Ala
XM_011540046.1:c.6950G>C	XP_011538348.1:p.Gly2317Ala
XM_011540047.1:c.6308G>C	XP_011538349.1:p.Gly2103Ala
XM_011540052.1:c.3818G>C	XP_011538354.1:p.Gly1273Ala
NM_022124.6:c.7295G>C MANE Select	NP_071407.4:p.Gly2432Ala