Canonical Allele Identifier: CA2663620408

Gene: CHRND

Linked Data

• gnomAD v4: 2-232528248-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528248C>A , CM000664.2:g.232528248C>A	GRCh38
NC_000002.11:g.233392958C>A , CM000664.1:g.233392958C>A	GRCh37
NC_000002.10:g.233101202C>A	NCBI36
NG_008028.1:g.7037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.244-14C>A MANE Select	ENSP00000258385.3:n.244-14C>A
ENST00000258385.7:c.244-14C>A	ENSP00000258385.3:n.244-14C>A
ENST00000412233.5:c.244-14C>A	ENSP00000398143.1:n.244-14C>A
ENST00000441621.6:c.244-14C>A	ENSP00000408819.2:n.244-14C>A
ENST00000446616.1:c.244-14C>A	ENSP00000410801.1:n.244-14C>A
ENST00000449596.5:c.199-14C>A	ENSP00000404950.1:n.199-14C>A
ENST00000543200.5:c.199-14C>A	ENSP00000438380.1:n.199-14C>A
NM_000751.2:c.244-14C>A	NP_000742.1:n.244-14C>A
NM_001256657.1:c.199-14C>A	NP_001243586.1:n.199-14C>A
NM_001311195.1:c.-28-14C>A	NP_001298124.1:n.-28-14C>A
NM_001311196.1:c.-28-14C>A	NP_001298125.1:n.-28-14C>A
NR_046333.1:c.-4294966996-14C>A
NR_046334.1:c.-4294966996-14C>A
XM_011510524.1:c.-28-14C>A	XP_011508826.1:n.-28-14C>A
XM_011510524.2:c.-28-14C>A	XP_011508826.1:n.-28-14C>A
NM_000751.3:c.244-14C>A MANE Select	NP_000742.1:n.244-14C>A
NM_001311195.2:c.-28-14C>A	NP_001298124.1:n.-28-14C>A
NM_001311196.2:c.-28-14C>A	NP_001298125.1:n.-28-14C>A
NM_001256657.2:c.199-14C>A	NP_001243586.1:n.199-14C>A