Canonical Allele Identifier: CA5696207

Gene: CASP7

Linked Data

• dbSNP Id: rs372133111
• ExAC: 10:115457334 C / A
• gnomAD v2: 10-115457334-C-A
• MyVariant Identifiers: chr10:g.115457334C>A (hg19) ; chr10:g.113697575C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113697575C>A , CM000672.2:g.113697575C>A	GRCh38
NC_000010.10:g.115457334C>A , CM000672.1:g.115457334C>A	GRCh37
NC_000010.9:g.115447324C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369318.8:c.82C>A MANE Select	ENSP00000358324.4:p.Arg28=
ENST00000345633.8:c.82C>A	ENSP00000298701.7:p.Arg28=
ENST00000369315.5:c.82C>A	ENSP00000358321.1:p.Arg28=
ENST00000369318.7:c.82C>A	ENSP00000358324.3:p.Arg28=
ENST00000369321.6:c.306C>A	ENSP00000358327.3:p.Thr102=
ENST00000369331.8:c.82C>A	ENSP00000358337.3:p.Arg28=
ENST00000429617.5:c.82C>A	ENSP00000400094.1:p.Arg28=
ENST00000614447.4:c.82C>A	ENSP00000478285.1:p.Arg28=
ENST00000621345.4:c.82C>A	ENSP00000480584.1:p.Arg28=
ENST00000621607.4:c.181C>A	ENSP00000478999.1:p.Arg61=
NM_001227.4:c.82C>A	NP_001218.1:p.Arg28=
NM_001267056.1:c.82C>A	NP_001253985.1:p.Arg28=
NM_001267057.1:c.306C>A	NP_001253986.1:p.Thr102=
NM_033338.5:c.181C>A	NP_203124.1:p.Arg61=
NM_033339.4:c.82C>A	NP_203125.1:p.Arg28=
NM_033340.3:c.82C>A	NP_203126.1:p.Arg28=
XM_006718017.2:c.93C>A	XP_006718080.1:p.Thr31=
XM_006718018.1:c.75C>A	XP_006718081.1:p.Thr25=
XM_011540259.1:c.181C>A	XP_011538561.1:p.Arg61=
NM_001320911.1:c.75C>A	NP_001307840.1:p.Thr25=
XM_006718017.3:c.93C>A	XP_006718080.1:p.Thr31=
XM_017016763.1:c.139C>A	XP_016872252.1:p.Arg47=
XM_017016764.1:c.75C>A	XP_016872253.1:p.Thr25=
NM_001227.5:c.82C>A MANE Select	NP_001218.1:p.Arg28=
NM_001320911.2:c.75C>A	NP_001307840.1:p.Thr25=
NM_033338.6:c.181C>A	NP_203124.1:p.Arg61=
NM_033339.5:c.82C>A	NP_203125.1:p.Arg28=
NM_033340.4:c.82C>A	NP_203126.1:p.Arg28=
NM_001267056.2:c.82C>A	NP_001253985.1:p.Arg28=