Canonical Allele Identifier: CA1335314100

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534305T= , CM000664.2:g.232534305T=	GRCh38
NC_000002.11:g.233399015T= , CM000664.1:g.233399015T=	GRCh37
NC_000002.10:g.233107259T=	NCBI36
NG_008028.1:g.13094T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1334T= MANE Select	ENSP00000258385.3:p.Ile445=
ENST00000258385.7:c.1334T=	ENSP00000258385.3:p.Ile445=
ENST00000441621.6:c.*516T=	ENSP00000408819.2:n.*516T=
ENST00000446616.1:c.*975T=	ENSP00000410801.1:n.*975T=
ENST00000543200.5:c.1289T=	ENSP00000438380.1:p.Ile430=
NM_000751.2:c.1334T=	NP_000742.1:p.Ile445=
NM_001256657.1:c.1289T=	NP_001243586.1:p.Ile430=
NM_001311195.1:c.752T=	NP_001298124.1:p.Ile251=
NM_001311196.1:c.1031T=	NP_001298125.1:p.Ile344=
NR_046333.1:c.-4294966217T=
NR_046334.1:c.-4294965938T=
XM_011510524.1:c.953T=	XP_011508826.1:p.Ile318=
XM_011510524.2:c.953T=	XP_011508826.1:p.Ile318=
NM_000751.3:c.1334T= MANE Select	NP_000742.1:p.Ile445=
NM_001311195.2:c.752T=	NP_001298124.1:p.Ile251=
NM_001311196.2:c.1031T=	NP_001298125.1:p.Ile344=
NM_001256657.2:c.1289T=	NP_001243586.1:p.Ile430=