Canonical Allele Identifier: CA351005436

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534232-C-T
• COSMIC: COSM6157092
• MyVariant Identifiers: chr2:g.233398942C>T (hg19) ; chr2:g.232534232C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534232C>T , CM000664.2:g.232534232C>T	GRCh38
NC_000002.11:g.233398942C>T , CM000664.1:g.233398942C>T	GRCh37
NC_000002.10:g.233107186C>T	NCBI36
NG_008028.1:g.13021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1261C>T MANE Select	ENSP00000258385.3:p.Pro421Ser
ENST00000258385.7:c.1261C>T	ENSP00000258385.3:p.Pro421Ser
ENST00000441621.6:c.*443C>T	ENSP00000408819.2:n.*443C>T
ENST00000446616.1:c.*902C>T	ENSP00000410801.1:n.*902C>T
ENST00000543200.5:c.1216C>T	ENSP00000438380.1:p.Pro406Ser
NM_000751.2:c.1261C>T	NP_000742.1:p.Pro421Ser
NM_001256657.1:c.1216C>T	NP_001243586.1:p.Pro406Ser
NM_001311195.1:c.679C>T	NP_001298124.1:p.Pro227Ser
NM_001311196.1:c.958C>T	NP_001298125.1:p.Pro320Ser
NR_046333.1:c.-4294966290C>T
NR_046334.1:c.-4294966011C>T
XM_011510524.1:c.880C>T	XP_011508826.1:p.Pro294Ser
XM_011510524.2:c.880C>T	XP_011508826.1:p.Pro294Ser
NM_000751.3:c.1261C>T MANE Select	NP_000742.1:p.Pro421Ser
NM_001311195.2:c.679C>T	NP_001298124.1:p.Pro227Ser
NM_001311196.2:c.958C>T	NP_001298125.1:p.Pro320Ser
NM_001256657.2:c.1216C>T	NP_001243586.1:p.Pro406Ser