Canonical Allele Identifier: CA351005447

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398945G>T (hg19) ; chr2:g.232534235G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534235G>T , CM000664.2:g.232534235G>T	GRCh38
NC_000002.11:g.233398945G>T , CM000664.1:g.233398945G>T	GRCh37
NC_000002.10:g.233107189G>T	NCBI36
NG_008028.1:g.13024G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1264G>T MANE Select	ENSP00000258385.3:p.Ala422Ser
ENST00000258385.7:c.1264G>T	ENSP00000258385.3:p.Ala422Ser
ENST00000441621.6:c.*446G>T	ENSP00000408819.2:n.*446G>T
ENST00000446616.1:c.*905G>T	ENSP00000410801.1:n.*905G>T
ENST00000543200.5:c.1219G>T	ENSP00000438380.1:p.Ala407Ser
NM_000751.2:c.1264G>T	NP_000742.1:p.Ala422Ser
NM_001256657.1:c.1219G>T	NP_001243586.1:p.Ala407Ser
NM_001311195.1:c.682G>T	NP_001298124.1:p.Ala228Ser
NM_001311196.1:c.961G>T	NP_001298125.1:p.Ala321Ser
NR_046333.1:c.-4294966287G>T
NR_046334.1:c.-4294966008G>T
XM_011510524.1:c.883G>T	XP_011508826.1:p.Ala295Ser
XM_011510524.2:c.883G>T	XP_011508826.1:p.Ala295Ser
NM_000751.3:c.1264G>T MANE Select	NP_000742.1:p.Ala422Ser
NM_001311195.2:c.682G>T	NP_001298124.1:p.Ala228Ser
NM_001311196.2:c.961G>T	NP_001298125.1:p.Ala321Ser
NM_001256657.2:c.1219G>T	NP_001243586.1:p.Ala407Ser