Canonical Allele Identifier: CA2205507

Gene: CAPN10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240591948C>T , CM000664.2:g.240591948C>T	GRCh38
NC_000002.11:g.241531365C>T , CM000664.1:g.241531365C>T	GRCh37
NC_000002.10:g.241180038C>T	NCBI36
NG_011558.2:g.10233C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391984.7:c.486C>T MANE Select	ENSP00000375844.2:p.Tyr162=
ENST00000270361.15:c.475C>T	ENSP00000270361.11:p.Arg159Ter
ENST00000270364.11:c.273+2474C>T	ENSP00000270364.7:n.273+2474C>T
ENST00000352879.8:c.141+4896C>T	ENSP00000289381.6:n.141+4896C>T
ENST00000354082.8:c.486C>T	ENSP00000270362.6:p.Tyr162=
ENST00000357048.8:c.486C>T	ENSP00000349556.4:p.Tyr162=
ENST00000391983.7:c.486C>T	ENSP00000375843.3:p.Tyr162=
ENST00000391984.6:c.486C>T	ENSP00000375844.2:p.Tyr162=
ENST00000404753.7:c.486C>T	ENSP00000384422.3:p.Tyr162=
ENST00000416591.5:c.486C>T	ENSP00000400144.1:p.Tyr162=
ENST00000432084.2:c.36C>T	ENSP00000407090.2:p.Tyr12=
ENST00000494738.5:n.2065C>T
NM_023083.3:c.486C>T	NP_075571.1:p.Tyr162=
NM_023085.3:c.486C>T	NP_075573.2:p.Tyr162=
NM_023083.4:c.486C>T MANE Select	NP_075571.2:p.Tyr162=
NM_023085.4:c.486C>T	NP_075573.3:p.Tyr162=