Canonical Allele Identifier: CA7357113

Gene: CINP

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102348705C>T , CM000676.2:g.102348705C>T	GRCh38
NC_000014.8:g.102815042C>T , CM000676.1:g.102815042C>T	GRCh37
NC_000014.7:g.101884795C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032630.3:c.491G>A MANE Select	NP_116019.1:p.Arg164His
ENST00000216756.11:c.491G>A MANE Select	ENSP00000216756.6:p.Arg164His
NM_001320046.1:c.*4G>A	NP_001306975.1:n.*4G>A
NM_001320046.2:c.*4G>A	NP_001306975.1:n.*4G>A
NM_032630.2:c.491G>A	NP_116019.1:p.Arg164His
ENST00000216756.10:c.491G>A	ENSP00000216756.6:p.Arg164His
ENST00000536961.6:c.536G>A	ENSP00000442057.2:p.Arg179His
ENST00000541568.6:c.*4G>A	ENSP00000442377.2:n.*4G>A
ENST00000559504.5:c.492G>A
ENST00000559514.5:c.491G>A	ENSP00000453839.1:p.Arg164His
XM_005267753.1:c.*4G>A	XP_005267810.1:n.*4G>A
XM_011536830.1:c.536G>A	XP_011535132.1:p.Arg179His
XM_011536831.1:c.*4G>A	XP_011535133.1:n.*4G>A