Canonical Allele Identifier: CA2053215

Gene: CASP10

Linked Data

• dbSNP Id: rs769715266
• ExAC: 2:202074160 TC / T
• gnomAD v2: 2-202074160-TC-T
• MyVariant Identifiers: chr2:g.202074161del (hg19) ; chr2:g.201209438del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209439del , CM000664.2:g.201209439del	GRCh38
NC_000002.11:g.202074162del , CM000664.1:g.202074162del	GRCh37
NC_000002.10:g.201782407del	NCBI36
NG_007265.1:g.31308del , LRG_33:g.31308del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1091del	ENSP00000314599.7:p.Pro364LeufsTer?
ENST00000346817.10:c.1163del	ENSP00000237865.7:p.Pro388LeufsTer?
ENST00000438843.6:c.*749del	ENSP00000401914.1:n.*749del
ENST00000492363.6:c.*378del	ENSP00000512459.1:n.*378del
ENST00000696199.1:c.721+5673del	ENSP00000512481.1:n.721+5673del
ENST00000286186.11:c.1292del MANE Select	ENSP00000286186.6:p.Pro431LeufsTer?
ENST00000272879.9:c.1292del	ENSP00000272879.5:p.Pro431LeufsTer?
ENST00000286186.10:c.1292del	ENSP00000286186.6:p.Pro431LeufsTer?
ENST00000313728.11:c.1091del	ENSP00000314599.7:p.Pro364LeufsTer?
ENST00000346817.9:c.1163del	ENSP00000237865.7:p.Pro388LeufsTer?
ENST00000360132.7:c.*378del	ENSP00000353250.3:n.*378del
ENST00000448480.1:c.1163del	ENSP00000396835.1:p.Pro388LeufsTer?
ENST00000492363.5:n.1200del
NM_001206524.1:c.1091del	NP_001193453.1:p.Pro364LeufsTer?
NM_001206542.1:c.1163del	NP_001193471.1:p.Pro388LeufsTer?
NM_001230.4:c.1163del	NP_001221.2:p.Pro388LeufsTer?
NM_032974.4:c.1292del	NP_116756.2:p.Pro431LeufsTer?
NM_032976.3:c.*378del	NP_116758.1:n.*378del
NM_032977.3:c.1292del , LRG_33t1:c.1292del	NP_116759.2:p.Pro431LeufsTer?
XM_005246907.2:c.1289del	XP_005246964.1:p.Pro430LeufsTer?
XM_006712796.2:c.542del	XP_006712859.1:p.Pro181LeufsTer?
XM_006712796.3:c.542del	XP_006712859.1:p.Pro181LeufsTer?
NM_001206524.2:c.1091del	NP_001193453.1:p.Pro364LeufsTer?
NM_001206542.2:c.1163del	NP_001193471.1:p.Pro388LeufsTer?
NM_001230.5:c.1163del	NP_001221.2:p.Pro388LeufsTer?
NM_032974.5:c.1292del	NP_116756.2:p.Pro431LeufsTer?
NM_032977.4:c.1292del MANE Select	NP_116759.2:p.Pro431LeufsTer?
NM_032976.4:c.*378del	NP_116758.1:n.*378del