Canonical Allele Identifier: CA5633449

Gene: ANKRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97572774C>T , CM000672.2:g.97572774C>T	GRCh38
NC_000010.10:g.99332531C>T , CM000672.1:g.99332531C>T	GRCh37
NC_000010.9:g.99322521C>T	NCBI36
NG_034079.1:g.5334C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298808.9:c.67C>T	ENSP00000298808.5:p.Pro23Ser
ENST00000307518.9:c.67C>T	ENSP00000306163.5:p.Pro23Ser
ENST00000370655.5:c.-15C>T	ENSP00000359689.1:n.-15C>T
NM_001129981.2:c.67C>T	NP_001123453.1:p.Pro23Ser
NM_001291218.1:c.325C>T	NP_001278147.1:p.Pro109Ser
NM_001291219.1:c.325C>T	NP_001278148.1:p.Pro109Ser
NM_020349.3:c.67C>T	NP_065082.2:p.Pro23Ser
NM_001291219.2:c.-15C>T	NP_001278148.2:n.-15C>T
NM_001346793.1:c.-15C>T	NP_001333722.1:n.-15C>T
NM_001346797.1:c.-15C>T	NP_001333726.1:n.-15C>T
NM_001129981.3:c.67C>T	NP_001123453.1:p.Pro23Ser
NM_020349.4:c.67C>T	NP_065082.2:p.Pro23Ser
NM_001291218.2:c.325C>T	NP_001278147.1:p.Pro109Ser