Canonical Allele Identifier: CA2663623939

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534351-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534351C>T , CM000664.2:g.232534351C>T	GRCh38
NC_000002.11:g.233399061C>T , CM000664.1:g.233399061C>T	GRCh37
NC_000002.10:g.233107305C>T	NCBI36
NG_008028.1:g.13140C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1371+9C>T MANE Select	ENSP00000258385.3:n.1371+9C>T
ENST00000258385.7:c.1371+9C>T	ENSP00000258385.3:n.1371+9C>T
ENST00000441621.6:c.*553+9C>T	ENSP00000408819.2:n.*553+9C>T
ENST00000446616.1:c.*1012+9C>T	ENSP00000410801.1:n.*1012+9C>T
ENST00000543200.5:c.1326+9C>T	ENSP00000438380.1:n.1326+9C>T
NM_000751.2:c.1371+9C>T	NP_000742.1:n.1371+9C>T
NM_001256657.1:c.1326+9C>T	NP_001243586.1:n.1326+9C>T
NM_001311195.1:c.789+9C>T	NP_001298124.1:n.789+9C>T
NM_001311196.1:c.1068+9C>T	NP_001298125.1:n.1068+9C>T
NR_046333.1:c.-4294966180+9C>T
NR_046334.1:c.-4294965901+9C>T
XM_011510524.1:c.990+9C>T	XP_011508826.1:n.990+9C>T
XM_011510524.2:c.990+9C>T	XP_011508826.1:n.990+9C>T
NM_000751.3:c.1371+9C>T MANE Select	NP_000742.1:n.1371+9C>T
NM_001311195.2:c.789+9C>T	NP_001298124.1:n.789+9C>T
NM_001311196.2:c.1068+9C>T	NP_001298125.1:n.1068+9C>T
NM_001256657.2:c.1326+9C>T	NP_001243586.1:n.1326+9C>T