Canonical Allele Identifier: CA1335314078

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534248_232534249delinsAG , CM000664.2:g.232534248_232534249delinsAG	GRCh38
NC_000002.11:g.233398958_233398959delinsAG , CM000664.1:g.233398958_233398959delinsAG	GRCh37
NC_000002.10:g.233107202_233107203delinsAG	NCBI36
NG_008028.1:g.13037_13038delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1277_1278delinsAG MANE Select	ENSP00000258385.3:p.Gln426=
ENST00000258385.7:c.1277_1278delinsAG	ENSP00000258385.3:p.Gln426=
ENST00000441621.6:c.*459_*460delinsAG	ENSP00000408819.2:n.*459_*460delinsAG
ENST00000446616.1:c.*918_*919delinsAG	ENSP00000410801.1:n.*918_*919delinsAG
ENST00000543200.5:c.1232_1233delinsAG	ENSP00000438380.1:p.Gln411=
NM_000751.2:c.1277_1278delinsAG	NP_000742.1:p.Gln426=
NM_001256657.1:c.1232_1233delinsAG	NP_001243586.1:p.Gln411=
NM_001311195.1:c.695_696delinsAG	NP_001298124.1:p.Gln232=
NM_001311196.1:c.974_975delinsAG	NP_001298125.1:p.Gln325=
NR_046333.1:c.-4294966274_-4294966273delinsAG
NR_046334.1:c.-4294965995_-4294965994delinsAG
XM_011510524.1:c.896_897delinsAG	XP_011508826.1:p.Gln299=
XM_011510524.2:c.896_897delinsAG	XP_011508826.1:p.Gln299=
NM_000751.3:c.1277_1278delinsAG MANE Select	NP_000742.1:p.Gln426=
NM_001311195.2:c.695_696delinsAG	NP_001298124.1:p.Gln232=
NM_001311196.2:c.974_975delinsAG	NP_001298125.1:p.Gln325=
NM_001256657.2:c.1232_1233delinsAG	NP_001243586.1:p.Gln411=