Canonical Allele Identifier: CA377143342

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468933C>G (hg19) ; chr10:g.71709176C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709176C>G , CM000672.2:g.71709176C>G	GRCh38
NC_000010.10:g.73468933C>G , CM000672.1:g.73468933C>G	GRCh37
NC_000010.9:g.73138939C>G	NCBI36
NG_008835.1:g.317230C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.3185C>G MANE Select	ENSP00000224721.9:p.Thr1062Ser
ENST00000398809.9:c.3185C>G	ENSP00000381789.5:p.Thr1062Ser
ENST00000442677.4:c.3185C>G	ENSP00000388894.3:p.Thr1062Ser
ENST00000466757.8:c.2616C>G
ENST00000224721.10:c.3200C>G	ENSP00000224721.8:p.Thr1067Ser
ENST00000398809.8:c.3185C>G	ENSP00000381789.5:p.Thr1062Ser
ENST00000442677.3:c.1960C>G
ENST00000466757.7:c.2616C>G
ENST00000616684.4:c.3185C>G	ENSP00000482036.2:p.Thr1062Ser
ENST00000622827.4:c.3185C>G	ENSP00000483211.1:p.Thr1062Ser
NM_001171930.1:c.3185C>G	NP_001165401.1:p.Thr1062Ser
NM_022124.5:c.3185C>G	NP_071407.4:p.Thr1062Ser
XM_006717940.2:c.3380C>G	XP_006718003.1:p.Thr1127Ser
XM_006717942.2:c.3314C>G	XP_006718005.1:p.Thr1105Ser
XM_011540039.1:c.3380C>G	XP_011538341.1:p.Thr1127Ser
XM_011540040.1:c.3374C>G	XP_011538342.1:p.Thr1125Ser
XM_011540041.1:c.3320C>G	XP_011538343.1:p.Thr1107Ser
XM_011540042.1:c.3380C>G	XP_011538344.1:p.Thr1127Ser
XM_011540043.1:c.3380C>G	XP_011538345.1:p.Thr1127Ser
XM_011540044.1:c.3245C>G	XP_011538346.1:p.Thr1082Ser
XM_011540045.1:c.3380C>G	XP_011538347.1:p.Thr1127Ser
XM_011540046.1:c.2840C>G	XP_011538348.1:p.Thr947Ser
XM_011540047.1:c.2198C>G	XP_011538349.1:p.Thr733Ser
XM_011540048.1:c.3380C>G	XP_011538350.1:p.Thr1127Ser
XM_011540049.1:c.3380C>G	XP_011538351.1:p.Thr1127Ser
XM_011540050.1:c.3380C>G	XP_011538352.1:p.Thr1127Ser
XM_011540051.1:c.3380C>G	XP_011538353.1:p.Thr1127Ser
XM_011540053.1:c.3380C>G	XP_011538355.1:p.Thr1127Ser
XR_945796.1:n.3623C>G
NM_001171930.2:c.3185C>G	NP_001165401.1:p.Thr1062Ser
NM_022124.6:c.3185C>G MANE Select	NP_071407.4:p.Thr1062Ser