Canonical Allele Identifier: CA377143338

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468932A>T (hg19) ; chr10:g.71709175A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709175A>T , CM000672.2:g.71709175A>T	GRCh38
NC_000010.10:g.73468932A>T , CM000672.1:g.73468932A>T	GRCh37
NC_000010.9:g.73138938A>T	NCBI36
NG_008835.1:g.317229A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.3184A>T MANE Select	ENSP00000224721.9:p.Thr1062Ser
ENST00000398809.9:c.3184A>T	ENSP00000381789.5:p.Thr1062Ser
ENST00000442677.4:c.3184A>T	ENSP00000388894.3:p.Thr1062Ser
ENST00000466757.8:c.2615A>T
ENST00000224721.10:c.3199A>T	ENSP00000224721.8:p.Thr1067Ser
ENST00000398809.8:c.3184A>T	ENSP00000381789.5:p.Thr1062Ser
ENST00000442677.3:c.1959A>T
ENST00000466757.7:c.2615A>T
ENST00000616684.4:c.3184A>T	ENSP00000482036.2:p.Thr1062Ser
ENST00000622827.4:c.3184A>T	ENSP00000483211.1:p.Thr1062Ser
NM_001171930.1:c.3184A>T	NP_001165401.1:p.Thr1062Ser
NM_022124.5:c.3184A>T	NP_071407.4:p.Thr1062Ser
XM_006717940.2:c.3379A>T	XP_006718003.1:p.Thr1127Ser
XM_006717942.2:c.3313A>T	XP_006718005.1:p.Thr1105Ser
XM_011540039.1:c.3379A>T	XP_011538341.1:p.Thr1127Ser
XM_011540040.1:c.3373A>T	XP_011538342.1:p.Thr1125Ser
XM_011540041.1:c.3319A>T	XP_011538343.1:p.Thr1107Ser
XM_011540042.1:c.3379A>T	XP_011538344.1:p.Thr1127Ser
XM_011540043.1:c.3379A>T	XP_011538345.1:p.Thr1127Ser
XM_011540044.1:c.3244A>T	XP_011538346.1:p.Thr1082Ser
XM_011540045.1:c.3379A>T	XP_011538347.1:p.Thr1127Ser
XM_011540046.1:c.2839A>T	XP_011538348.1:p.Thr947Ser
XM_011540047.1:c.2197A>T	XP_011538349.1:p.Thr733Ser
XM_011540048.1:c.3379A>T	XP_011538350.1:p.Thr1127Ser
XM_011540049.1:c.3379A>T	XP_011538351.1:p.Thr1127Ser
XM_011540050.1:c.3379A>T	XP_011538352.1:p.Thr1127Ser
XM_011540051.1:c.3379A>T	XP_011538353.1:p.Thr1127Ser
XM_011540053.1:c.3379A>T	XP_011538355.1:p.Thr1127Ser
XR_945796.1:n.3622A>T
NM_001171930.2:c.3184A>T	NP_001165401.1:p.Thr1062Ser
NM_022124.6:c.3184A>T MANE Select	NP_071407.4:p.Thr1062Ser