Canonical Allele Identifier: CA377155179

Gene: CDH23

Linked Data

• gnomAD v4: 10-71793421-G-C
• MyVariant Identifiers: chr10:g.73553178G>C (hg19) ; chr10:g.71793421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793421G>C , CM000672.2:g.71793421G>C	GRCh38
NC_000010.10:g.73553178G>C , CM000672.1:g.73553178G>C	GRCh37
NC_000010.9:g.73223184G>C	NCBI36
NG_008835.1:g.401475G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6493G>C MANE Select	ENSP00000224721.9:p.Asp2165His
ENST00000224721.10:c.6508G>C	ENSP00000224721.8:p.Asp2170His
ENST00000622827.4:c.6493G>C	ENSP00000483211.1:p.Asp2165His
NM_022124.5:c.6493G>C	NP_071407.4:p.Asp2165His
XM_006717940.2:c.6688G>C	XP_006718003.1:p.Asp2230His
XM_006717942.2:c.6622G>C	XP_006718005.1:p.Asp2208His
XM_011540039.1:c.6685G>C	XP_011538341.1:p.Asp2229His
XM_011540040.1:c.6682G>C	XP_011538342.1:p.Asp2228His
XM_011540041.1:c.6628G>C	XP_011538343.1:p.Asp2210His
XM_011540042.1:c.6598G>C	XP_011538344.1:p.Asp2200His
XM_011540043.1:c.6688G>C	XP_011538345.1:p.Asp2230His
XM_011540044.1:c.6553G>C	XP_011538346.1:p.Asp2185His
XM_011540045.1:c.6688G>C	XP_011538347.1:p.Asp2230His
XM_011540046.1:c.6148G>C	XP_011538348.1:p.Asp2050His
XM_011540047.1:c.5506G>C	XP_011538349.1:p.Asp1836His
XM_011540048.1:c.6688G>C	XP_011538350.1:p.Asp2230His
XM_011540049.1:c.6688G>C	XP_011538351.1:p.Asp2230His
XM_011540050.1:c.6688G>C	XP_011538352.1:p.Asp2230His
XM_011540051.1:c.6688G>C	XP_011538353.1:p.Asp2230His
XM_011540052.1:c.3016G>C	XP_011538354.1:p.Asp1006His
XR_945796.1:n.6931G>C
NM_022124.6:c.6493G>C MANE Select	NP_071407.4:p.Asp2165His