Canonical Allele Identifier: CA596113004

Gene: CASP7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113679885del , CM000672.2:g.113679885del	GRCh38
NC_000010.10:g.115439644del , CM000672.1:g.115439644del	GRCh37
NC_000010.9:g.115429634del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345633.8:c.-168del	ENSP00000298701.7:n.-168del
ENST00000369318.7:c.-94del	ENSP00000358324.3:n.-94del
ENST00000369321.6:c.131del	ENSP00000358327.3:p.Leu44Ter
ENST00000369331.8:c.-1+536del	ENSP00000358337.3:n.-1+536del
ENST00000429617.5:c.-1+536del	ENSP00000400094.1:n.-1+536del
ENST00000614447.4:c.-94del	ENSP00000478285.1:n.-94del
ENST00000621345.4:c.-1+536del	ENSP00000480584.1:n.-1+536del
NM_001227.4:c.-94del	NP_001218.1:n.-94del
NM_001267056.1:c.-1+536del	NP_001253985.1:n.-1+536del
NM_001267057.1:c.131del	NP_001253986.1:p.Leu44Ter
NM_033338.5:c.-102del	NP_203124.1:n.-102del
NM_033339.4:c.-168del	NP_203125.1:n.-168del
NM_033340.3:c.-1+536del	NP_203126.1:n.-1+536del
XM_006718018.1:c.-8+536del	XP_006718081.1:n.-8+536del
NM_001320911.1:c.-8+536del	NP_001307840.1:n.-8+536del
NM_001320911.2:c.-8+536del	NP_001307840.1:n.-8+536del
NM_033340.4:c.-1+536del	NP_203126.1:n.-1+536del
NM_001267056.2:c.-1+536del	NP_001253985.1:n.-1+536del