Canonical Allele Identifier: CA431952535

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398748C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534038C>G , CM000664.2:g.232534038C>G	GRCh38
NC_000002.11:g.233398748C>G , CM000664.1:g.233398748C>G	GRCh37
NC_000002.10:g.233106992C>G	NCBI36
NG_008028.1:g.12827C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1155C>G MANE Select	ENSP00000258385.3:p.Ser385=
ENST00000258385.7:c.1155C>G	ENSP00000258385.3:p.Ser385=
ENST00000441621.6:c.*337C>G	ENSP00000408819.2:n.*337C>G
ENST00000446616.1:c.*796C>G	ENSP00000410801.1:n.*796C>G
ENST00000543200.5:c.1110C>G	ENSP00000438380.1:p.Ser370=
NM_000751.2:c.1155C>G	NP_000742.1:p.Ser385=
NM_001256657.1:c.1110C>G	NP_001243586.1:p.Ser370=
NM_001311195.1:c.573C>G	NP_001298124.1:p.Ser191=
NM_001311196.1:c.852C>G	NP_001298125.1:p.Ser284=
NR_046333.1:c.-4294966396C>G
NR_046334.1:c.-4294966117C>G
XM_011510524.1:c.774C>G	XP_011508826.1:p.Ser258=
XM_011510524.2:c.774C>G	XP_011508826.1:p.Ser258=
NM_000751.3:c.1155C>G MANE Select	NP_000742.1:p.Ser385=
NM_001311195.2:c.573C>G	NP_001298124.1:p.Ser191=
NM_001311196.2:c.852C>G	NP_001298125.1:p.Ser284=
NM_001256657.2:c.1110C>G	NP_001243586.1:p.Ser370=