Canonical Allele Identifier: CA1339191417

Gene: CAPN10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240591746T= , CM000664.2:g.240591746T=	GRCh38
NC_000002.11:g.241531163T= , CM000664.1:g.241531163T=	GRCh37
NC_000002.10:g.241179836T=	NCBI36
NG_011558.2:g.10031T=

Transcript Alleles

HGVS	Amino-acid Change
NM_023083.4:c.471-187T= MANE Select	NP_075571.2:n.471-187T=
ENST00000391984.7:c.471-187T= MANE Select	ENSP00000375844.2:n.471-187T=
NM_023083.3:c.471-187T=	NP_075571.1:n.471-187T=
NM_023085.3:c.471-187T=	NP_075573.2:n.471-187T=
NM_023085.4:c.471-187T=	NP_075573.3:n.471-187T=
ENST00000270361.15:c.460-187T=	ENSP00000270361.11:n.460-187T=
ENST00000270364.11:c.273+2272T=	ENSP00000270364.7:n.273+2272T=
ENST00000352879.8:c.141+4694T=	ENSP00000289381.6:n.141+4694T=
ENST00000354082.8:c.471-187T=	ENSP00000270362.6:n.471-187T=
ENST00000357048.8:c.471-187T=	ENSP00000349556.4:n.471-187T=
ENST00000391983.7:c.471-187T=	ENSP00000375843.3:n.471-187T=
ENST00000391984.6:c.471-187T=	ENSP00000375844.2:n.471-187T=
ENST00000404753.7:c.471-187T=	ENSP00000384422.3:n.471-187T=
ENST00000416591.5:c.471-187T=	ENSP00000400144.1:n.471-187T=
ENST00000432084.2:c.21-187T=	ENSP00000407090.2:n.21-187T=
ENST00000494738.5:n.1863T=