Canonical Allele Identifier: CA2663624000

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534376-T-TGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534376_232534377insGTA , CM000664.2:g.232534376_232534377insGTA	GRCh38
NC_000002.11:g.233399086_233399087insGTA , CM000664.1:g.233399086_233399087insGTA	GRCh37
NC_000002.10:g.233107330_233107331insGTA	NCBI36
NG_008028.1:g.13165_13166insGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1371+34_1371+35insGTA MANE Select	ENSP00000258385.3:n.1371+34_1371+35insGTA
ENST00000258385.7:c.1371+34_1371+35insGTA	ENSP00000258385.3:n.1371+34_1371+35insGTA
ENST00000441621.6:c.*553+34_*553+35insGTA	ENSP00000408819.2:n.*553+34_*553+35insGTA
ENST00000446616.1:c.*1012+34_*1012+35insGTA	ENSP00000410801.1:n.*1012+34_*1012+35insGTA
ENST00000543200.5:c.1326+34_1326+35insGTA	ENSP00000438380.1:n.1326+34_1326+35insGTA
NM_000751.2:c.1371+34_1371+35insGTA	NP_000742.1:n.1371+34_1371+35insGTA
NM_001256657.1:c.1326+34_1326+35insGTA	NP_001243586.1:n.1326+34_1326+35insGTA
NM_001311195.1:c.789+34_789+35insGTA	NP_001298124.1:n.789+34_789+35insGTA
NM_001311196.1:c.1068+34_1068+35insGTA	NP_001298125.1:n.1068+34_1068+35insGTA
NR_046333.1:c.-4294966180+34_-4294966180+35insGTA
NR_046334.1:c.-4294965901+34_-4294965901+35insGTA
XM_011510524.1:c.990+34_990+35insGTA	XP_011508826.1:n.990+34_990+35insGTA
XM_011510524.2:c.990+34_990+35insGTA	XP_011508826.1:n.990+34_990+35insGTA
NM_000751.3:c.1371+34_1371+35insGTA MANE Select	NP_000742.1:n.1371+34_1371+35insGTA
NM_001311195.2:c.789+34_789+35insGTA	NP_001298124.1:n.789+34_789+35insGTA
NM_001311196.2:c.1068+34_1068+35insGTA	NP_001298125.1:n.1068+34_1068+35insGTA
NM_001256657.2:c.1326+34_1326+35insGTA	NP_001243586.1:n.1326+34_1326+35insGTA