Canonical Allele Identifier: CA1335314102

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534315_232534317delinsCAT , CM000664.2:g.232534315_232534317delinsCAT	GRCh38
NC_000002.11:g.233399025_233399027delinsCAT , CM000664.1:g.233399025_233399027delinsCAT	GRCh37
NC_000002.10:g.233107269_233107271delinsCAT	NCBI36
NG_008028.1:g.13104_13106delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1344_1346delinsCAT MANE Select	ENSP00000258385.3:p.His448=
ENST00000258385.7:c.1344_1346delinsCAT	ENSP00000258385.3:p.His448=
ENST00000441621.6:c.*526_*528delinsCAT	ENSP00000408819.2:n.*526_*528delinsCAT
ENST00000446616.1:c.*985_*987delinsCAT	ENSP00000410801.1:n.*985_*987delinsCAT
ENST00000543200.5:c.1299_1301delinsCAT	ENSP00000438380.1:p.His433=
NM_000751.2:c.1344_1346delinsCAT	NP_000742.1:p.His448=
NM_001256657.1:c.1299_1301delinsCAT	NP_001243586.1:p.His433=
NM_001311195.1:c.762_764delinsCAT	NP_001298124.1:p.His254=
NM_001311196.1:c.1041_1043delinsCAT	NP_001298125.1:p.His347=
NR_046333.1:c.-4294966207_-4294966205delinsCAT
NR_046334.1:c.-4294965928_-4294965926delinsCAT
XM_011510524.1:c.963_965delinsCAT	XP_011508826.1:p.His321=
XM_011510524.2:c.963_965delinsCAT	XP_011508826.1:p.His321=
NM_000751.3:c.1344_1346delinsCAT MANE Select	NP_000742.1:p.His448=
NM_001311195.2:c.762_764delinsCAT	NP_001298124.1:p.His254=
NM_001311196.2:c.1041_1043delinsCAT	NP_001298125.1:p.His347=
NM_001256657.2:c.1299_1301delinsCAT	NP_001243586.1:p.His433=