Canonical Allele Identifier: CA377154963

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553109C>G (hg19) ; chr10:g.71793352C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793352C>G , CM000672.2:g.71793352C>G	GRCh38
NC_000010.10:g.73553109C>G , CM000672.1:g.73553109C>G	GRCh37
NC_000010.9:g.73223115C>G	NCBI36
NG_008835.1:g.401406C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6424C>G MANE Select	ENSP00000224721.9:p.Leu2142Val
ENST00000224721.10:c.6439C>G	ENSP00000224721.8:p.Leu2147Val
ENST00000622827.4:c.6424C>G	ENSP00000483211.1:p.Leu2142Val
NM_022124.5:c.6424C>G	NP_071407.4:p.Leu2142Val
XM_006717940.2:c.6619C>G	XP_006718003.1:p.Leu2207Val
XM_006717942.2:c.6553C>G	XP_006718005.1:p.Leu2185Val
XM_011540039.1:c.6616C>G	XP_011538341.1:p.Leu2206Val
XM_011540040.1:c.6613C>G	XP_011538342.1:p.Leu2205Val
XM_011540041.1:c.6559C>G	XP_011538343.1:p.Leu2187Val
XM_011540042.1:c.6577+42C>G	XP_011538344.1:n.6577+42C>G
XM_011540043.1:c.6619C>G	XP_011538345.1:p.Leu2207Val
XM_011540044.1:c.6484C>G	XP_011538346.1:p.Leu2162Val
XM_011540045.1:c.6619C>G	XP_011538347.1:p.Leu2207Val
XM_011540046.1:c.6079C>G	XP_011538348.1:p.Leu2027Val
XM_011540047.1:c.5437C>G	XP_011538349.1:p.Leu1813Val
XM_011540048.1:c.6619C>G	XP_011538350.1:p.Leu2207Val
XM_011540049.1:c.6619C>G	XP_011538351.1:p.Leu2207Val
XM_011540050.1:c.6619C>G	XP_011538352.1:p.Leu2207Val
XM_011540051.1:c.6619C>G	XP_011538353.1:p.Leu2207Val
XM_011540052.1:c.2947C>G	XP_011538354.1:p.Leu983Val
XR_945796.1:n.6862C>G
NM_022124.6:c.6424C>G MANE Select	NP_071407.4:p.Leu2142Val