Canonical Allele Identifier: CA378416604

Gene: CASP7

Linked Data

• MyVariant Identifiers: chr10:g.115457332A>T (hg19) ; chr10:g.113697573A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113697573A>T , CM000672.2:g.113697573A>T	GRCh38
NC_000010.10:g.115457332A>T , CM000672.1:g.115457332A>T	GRCh37
NC_000010.9:g.115447322A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369318.8:c.80A>T MANE Select	ENSP00000358324.4:p.Asp27Val
ENST00000345633.8:c.80A>T	ENSP00000298701.7:p.Asp27Val
ENST00000369315.5:c.80A>T	ENSP00000358321.1:p.Asp27Val
ENST00000369318.7:c.80A>T	ENSP00000358324.3:p.Asp27Val
ENST00000369321.6:c.304A>T	ENSP00000358327.3:p.Thr102Ser
ENST00000369331.8:c.80A>T	ENSP00000358337.3:p.Asp27Val
ENST00000429617.5:c.80A>T	ENSP00000400094.1:p.Asp27Val
ENST00000614447.4:c.80A>T	ENSP00000478285.1:p.Asp27Val
ENST00000621345.4:c.80A>T	ENSP00000480584.1:p.Asp27Val
ENST00000621607.4:c.179A>T	ENSP00000478999.1:p.Asp60Val
NM_001227.4:c.80A>T	NP_001218.1:p.Asp27Val
NM_001267056.1:c.80A>T	NP_001253985.1:p.Asp27Val
NM_001267057.1:c.304A>T	NP_001253986.1:p.Thr102Ser
NM_033338.5:c.179A>T	NP_203124.1:p.Asp60Val
NM_033339.4:c.80A>T	NP_203125.1:p.Asp27Val
NM_033340.3:c.80A>T	NP_203126.1:p.Asp27Val
XM_006718017.2:c.91A>T	XP_006718080.1:p.Thr31Ser
XM_006718018.1:c.73A>T	XP_006718081.1:p.Thr25Ser
XM_011540259.1:c.179A>T	XP_011538561.1:p.Asp60Val
NM_001320911.1:c.73A>T	NP_001307840.1:p.Thr25Ser
XM_006718017.3:c.91A>T	XP_006718080.1:p.Thr31Ser
XM_017016763.1:c.137A>T	XP_016872252.1:p.Asp46Val
XM_017016764.1:c.73A>T	XP_016872253.1:p.Thr25Ser
NM_001227.5:c.80A>T MANE Select	NP_001218.1:p.Asp27Val
NM_001320911.2:c.73A>T	NP_001307840.1:p.Thr25Ser
NM_033338.6:c.179A>T	NP_203124.1:p.Asp60Val
NM_033339.5:c.80A>T	NP_203125.1:p.Asp27Val
NM_033340.4:c.80A>T	NP_203126.1:p.Asp27Val
NM_001267056.2:c.80A>T	NP_001253985.1:p.Asp27Val