Canonical Allele Identifier: CA1335313964

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232533997G= , CM000664.2:g.232533997G=	GRCh38
NC_000002.11:g.233398707G= , CM000664.1:g.233398707G=	GRCh37
NC_000002.10:g.233106951G=	NCBI36
NG_008028.1:g.12786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1114G= MANE Select	ENSP00000258385.3:p.Gly372=
ENST00000258385.7:c.1114G=	ENSP00000258385.3:p.Gly372=
ENST00000441621.6:c.*296G=	ENSP00000408819.2:n.*296G=
ENST00000446616.1:c.*755G=	ENSP00000410801.1:n.*755G=
ENST00000543200.5:c.1069G=	ENSP00000438380.1:p.Gly357=
NM_000751.2:c.1114G=	NP_000742.1:p.Gly372=
NM_001256657.1:c.1069G=	NP_001243586.1:p.Gly357=
NM_001311195.1:c.532G=	NP_001298124.1:p.Gly178=
NM_001311196.1:c.811G=	NP_001298125.1:p.Gly271=
NR_046333.1:c.-4294966437G=
NR_046334.1:c.-4294966158G=
XM_011510524.1:c.733G=	XP_011508826.1:p.Gly245=
XM_011510524.2:c.733G=	XP_011508826.1:p.Gly245=
NM_000751.3:c.1114G= MANE Select	NP_000742.1:p.Gly372=
NM_001311195.2:c.532G=	NP_001298124.1:p.Gly178=
NM_001311196.2:c.811G=	NP_001298125.1:p.Gly271=
NM_001256657.2:c.1069G=	NP_001243586.1:p.Gly357=