Canonical Allele Identifier: CA430829598

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202074112A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209389A>C , CM000664.2:g.201209389A>C	GRCh38
NC_000002.11:g.202074112A>C , CM000664.1:g.202074112A>C	GRCh37
NC_000002.10:g.201782357A>C	NCBI36
NG_007265.1:g.31258A>C , LRG_33:g.31258A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313728.12:c.1041A>C	ENSP00000314599.7:p.Ala347=
ENST00000346817.10:c.1113A>C	ENSP00000237865.7:p.Ala371=
ENST00000438843.6:c.*699A>C	ENSP00000401914.1:n.*699A>C
ENST00000492363.6:c.*328A>C	ENSP00000512459.1:n.*328A>C
ENST00000696199.1:c.721+5623A>C	ENSP00000512481.1:n.721+5623A>C
ENST00000286186.11:c.1242A>C MANE Select	ENSP00000286186.6:p.Ala414=
ENST00000272879.9:c.1242A>C	ENSP00000272879.5:p.Ala414=
ENST00000286186.10:c.1242A>C	ENSP00000286186.6:p.Ala414=
ENST00000313728.11:c.1041A>C	ENSP00000314599.7:p.Ala347=
ENST00000346817.9:c.1113A>C	ENSP00000237865.7:p.Ala371=
ENST00000360132.7:c.*328A>C	ENSP00000353250.3:n.*328A>C
ENST00000448480.1:c.1113A>C	ENSP00000396835.1:p.Ala371=
ENST00000492363.5:n.1150A>C
NM_001206524.1:c.1041A>C	NP_001193453.1:p.Ala347=
NM_001206542.1:c.1113A>C	NP_001193471.1:p.Ala371=
NM_001230.4:c.1113A>C	NP_001221.2:p.Ala371=
NM_032974.4:c.1242A>C	NP_116756.2:p.Ala414=
NM_032976.3:c.*328A>C	NP_116758.1:n.*328A>C
NM_032977.3:c.1242A>C , LRG_33t1:c.1242A>C	NP_116759.2:p.Ala414=
XM_005246907.2:c.1239A>C	XP_005246964.1:p.Ala413=
XM_006712796.2:c.492A>C	XP_006712859.1:p.Ala164=
XM_006712796.3:c.492A>C	XP_006712859.1:p.Ala164=
NM_001206524.2:c.1041A>C	NP_001193453.1:p.Ala347=
NM_001206542.2:c.1113A>C	NP_001193471.1:p.Ala371=
NM_001230.5:c.1113A>C	NP_001221.2:p.Ala371=
NM_032974.5:c.1242A>C	NP_116756.2:p.Ala414=
NM_032977.4:c.1242A>C MANE Select	NP_116759.2:p.Ala414=
NM_032976.4:c.*328A>C	NP_116758.1:n.*328A>C