Canonical Allele Identifier: CA1335314101

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534310A= , CM000664.2:g.232534310A=	GRCh38
NC_000002.11:g.233399020A= , CM000664.1:g.233399020A=	GRCh37
NC_000002.10:g.233107264A=	NCBI36
NG_008028.1:g.13099A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1339A= MANE Select	ENSP00000258385.3:p.Asn447=
ENST00000258385.7:c.1339A=	ENSP00000258385.3:p.Asn447=
ENST00000441621.6:c.*521A=	ENSP00000408819.2:n.*521A=
ENST00000446616.1:c.*980A=	ENSP00000410801.1:n.*980A=
ENST00000543200.5:c.1294A=	ENSP00000438380.1:p.Asn432=
NM_000751.2:c.1339A=	NP_000742.1:p.Asn447=
NM_001256657.1:c.1294A=	NP_001243586.1:p.Asn432=
NM_001311195.1:c.757A=	NP_001298124.1:p.Asn253=
NM_001311196.1:c.1036A=	NP_001298125.1:p.Asn346=
NR_046333.1:c.-4294966212A=
NR_046334.1:c.-4294965933A=
XM_011510524.1:c.958A=	XP_011508826.1:p.Asn320=
XM_011510524.2:c.958A=	XP_011508826.1:p.Asn320=
NM_000751.3:c.1339A= MANE Select	NP_000742.1:p.Asn447=
NM_001311195.2:c.757A=	NP_001298124.1:p.Asn253=
NM_001311196.2:c.1036A=	NP_001298125.1:p.Asn346=
NM_001256657.2:c.1294A=	NP_001243586.1:p.Asn432=