Canonical Allele Identifier: CA1335310467

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528408C= , CM000664.2:g.232528408C=	GRCh38
NC_000002.11:g.233393118C= , CM000664.1:g.233393118C=	GRCh37
NC_000002.10:g.233101362C=	NCBI36
NG_008028.1:g.7197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.353+37C= MANE Select	ENSP00000258385.3:n.353+37C=
ENST00000258385.7:c.353+37C=	ENSP00000258385.3:n.353+37C=
ENST00000412233.5:c.353+37C=	ENSP00000398143.1:n.353+37C=
ENST00000441621.6:c.353+37C=	ENSP00000408819.2:n.353+37C=
ENST00000446616.1:c.321+69C=	ENSP00000410801.1:n.321+69C=
ENST00000449596.5:c.308+37C=	ENSP00000404950.1:n.308+37C=
ENST00000543200.5:c.308+37C=	ENSP00000438380.1:n.308+37C=
NM_000751.2:c.353+37C=	NP_000742.1:n.353+37C=
NM_001256657.1:c.308+37C=	NP_001243586.1:n.308+37C=
NM_001311195.1:c.82+37C=	NP_001298124.1:n.82+37C=
NM_001311196.1:c.50+69C=	NP_001298125.1:n.50+69C=
NR_046333.1:c.-4294966887+37C=
NR_046334.1:c.-4294966919+69C=
XM_011510524.1:c.82+37C=	XP_011508826.1:n.82+37C=
XM_011510524.2:c.82+37C=	XP_011508826.1:n.82+37C=
NM_000751.3:c.353+37C= MANE Select	NP_000742.1:n.353+37C=
NM_001311195.2:c.82+37C=	NP_001298124.1:n.82+37C=
NM_001311196.2:c.50+69C=	NP_001298125.1:n.50+69C=
NM_001256657.2:c.308+37C=	NP_001243586.1:n.308+37C=