Canonical Allele Identifier: CA2754657215

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528403_232528404del , CM000664.2:g.232528403_232528404del	GRCh38
NC_000002.11:g.233393113_233393114del , CM000664.1:g.233393113_233393114del	GRCh37
NC_000002.10:g.233101357_233101358del	NCBI36
NG_008028.1:g.7192_7193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.353+32_353+33del MANE Select	ENSP00000258385.3:n.353+32_353+33del
ENST00000258385.7:c.353+32_353+33del	ENSP00000258385.3:n.353+32_353+33del
ENST00000412233.5:c.353+32_353+33del	ENSP00000398143.1:n.353+32_353+33del
ENST00000441621.6:c.353+32_353+33del	ENSP00000408819.2:n.353+32_353+33del
ENST00000446616.1:c.321+64_321+65del	ENSP00000410801.1:n.321+64_321+65del
ENST00000449596.5:c.308+32_308+33del	ENSP00000404950.1:n.308+32_308+33del
ENST00000543200.5:c.308+32_308+33del	ENSP00000438380.1:n.308+32_308+33del
NM_000751.2:c.353+32_353+33del	NP_000742.1:n.353+32_353+33del
NM_001256657.1:c.308+32_308+33del	NP_001243586.1:n.308+32_308+33del
NM_001311195.1:c.82+32_82+33del	NP_001298124.1:n.82+32_82+33del
NM_001311196.1:c.50+64_50+65del	NP_001298125.1:n.50+64_50+65del
NR_046333.1:c.-4294966887+32_-4294966887+33del
NR_046334.1:c.-4294966919+64_-4294966919+65del
XM_011510524.1:c.82+32_82+33del	XP_011508826.1:n.82+32_82+33del
XM_011510524.2:c.82+32_82+33del	XP_011508826.1:n.82+32_82+33del
NM_000751.3:c.353+32_353+33del MANE Select	NP_000742.1:n.353+32_353+33del
NM_001311195.2:c.82+32_82+33del	NP_001298124.1:n.82+32_82+33del
NM_001311196.2:c.50+64_50+65del	NP_001298125.1:n.50+64_50+65del
NM_001256657.2:c.308+32_308+33del	NP_001243586.1:n.308+32_308+33del