Canonical Allele Identifier: CA1335313959

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232533987_232533988delinsAC , CM000664.2:g.232533987_232533988delinsAC	GRCh38
NC_000002.11:g.233398697_233398698delinsAC , CM000664.1:g.233398697_233398698delinsAC	GRCh37
NC_000002.10:g.233106941_233106942delinsAC	NCBI36
NG_008028.1:g.12776_12777delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1104_1105delinsAC MANE Select	ENSP00000258385.3:p.Gly368=
ENST00000258385.7:c.1104_1105delinsAC	ENSP00000258385.3:p.Gly368=
ENST00000441621.6:c.*286_*287delinsAC	ENSP00000408819.2:n.*286_*287delinsAC
ENST00000446616.1:c.*745_*746delinsAC	ENSP00000410801.1:n.*745_*746delinsAC
ENST00000543200.5:c.1059_1060delinsAC	ENSP00000438380.1:p.Gly353=
NM_000751.2:c.1104_1105delinsAC	NP_000742.1:p.Gly368=
NM_001256657.1:c.1059_1060delinsAC	NP_001243586.1:p.Gly353=
NM_001311195.1:c.522_523delinsAC	NP_001298124.1:p.Gly174=
NM_001311196.1:c.801_802delinsAC	NP_001298125.1:p.Gly267=
NR_046333.1:c.-4294966447_-4294966446delinsAC
NR_046334.1:c.-4294966168_-4294966167delinsAC
XM_011510524.1:c.723_724delinsAC	XP_011508826.1:p.Gly241=
XM_011510524.2:c.723_724delinsAC	XP_011508826.1:p.Gly241=
NM_000751.3:c.1104_1105delinsAC MANE Select	NP_000742.1:p.Gly368=
NM_001311195.2:c.522_523delinsAC	NP_001298124.1:p.Gly174=
NM_001311196.2:c.801_802delinsAC	NP_001298125.1:p.Gly267=
NM_001256657.2:c.1059_1060delinsAC	NP_001243586.1:p.Gly353=