Canonical Allele Identifier: CA2663623459

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534131-TGCACGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534133_232534139del , CM000664.2:g.232534133_232534139del	GRCh38
NC_000002.11:g.233398843_233398849del , CM000664.1:g.233398843_233398849del	GRCh37
NC_000002.10:g.233107087_233107093del	NCBI36
NG_008028.1:g.12922_12928del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1250_1252+4del
ENST00000258385.7:c.1250_1252+4del
ENST00000441621.6:c.*432_*434+4del
ENST00000446616.1:c.*891_*893+4del
ENST00000543200.5:c.1205_1207+4del
NM_000751.2:c.1250_1252+4del
NM_001256657.1:c.1205_1207+4del
NM_001311195.1:c.668_670+4del
NM_001311196.1:c.947_949+4del
NR_046333.1:c.-4294966301_-4294966299+4del
NR_046334.1:c.-4294966022_-4294966020+4del
XM_011510524.1:c.869_871+4del
XM_011510524.2:c.869_871+4del
NM_000751.3:c.1250_1252+4del
NM_001311195.2:c.668_670+4del
NM_001311196.2:c.947_949+4del
NM_001256657.2:c.1205_1207+4del