Canonical Allele Identifier: CA2615775272

Gene: CASP1

Linked Data

• gnomAD v4: 11-105027204-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105027204G>T , CM000673.2:g.105027204G>T	GRCh38
NC_000011.9:g.104897931G>T , CM000673.1:g.104897931G>T	GRCh37
NC_000011.8:g.104403141G>T	NCBI36
NG_029124.1:g.12927C>A
NG_029124.2:g.12927C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525825.6:c.944-253C>A	ENSP00000434779.1:n.944-253C>A
ENST00000532439.6:c.565-253C>A
ENST00000695714.1:c.*495-253C>A	ENSP00000512113.1:n.*495-253C>A
ENST00000695715.1:c.890-253C>A	ENSP00000512114.1:n.890-253C>A
ENST00000695716.1:c.*717-253C>A	ENSP00000512253.1:n.*717-253C>A
ENST00000695717.1:c.890-253C>A	ENSP00000512115.1:n.890-253C>A
ENST00000695718.1:c.890-253C>A	ENSP00000512116.1:n.890-253C>A
ENST00000695719.1:c.944-253C>A	ENSP00000512117.1:n.944-253C>A
ENST00000695720.1:c.1007-253C>A	ENSP00000512118.1:n.1007-253C>A
ENST00000695721.1:c.890-253C>A	ENSP00000512119.1:n.890-253C>A
ENST00000695722.1:c.890-253C>A	ENSP00000512120.1:n.890-253C>A
ENST00000533400.6:c.1007-253C>A MANE Select	ENSP00000433138.1:n.1007-253C>A
ENST00000353247.9:c.59-253C>A	ENSP00000344132.5:n.59-253C>A
ENST00000436863.7:c.1007-253C>A	ENSP00000410076.3:n.1007-253C>A
ENST00000446369.5:c.584-253C>A	ENSP00000403260.1:n.584-253C>A
ENST00000525825.5:c.944-253C>A	ENSP00000434779.1:n.944-253C>A
ENST00000526568.5:c.728-253C>A	ENSP00000434250.1:n.728-253C>A
ENST00000527979.5:c.896-253C>A	ENSP00000432340.1:n.896-253C>A
ENST00000528974.1:c.890-211C>A	ENSP00000434259.1:n.890-211C>A
ENST00000529871.1:c.*495-253C>A	ENSP00000431947.1:n.*495-253C>A
ENST00000531166.5:c.59-253C>A	ENSP00000434303.1:n.59-253C>A
ENST00000532439.5:c.554-253C>A	ENSP00000435536.1:n.554-253C>A
ENST00000533400.5:c.1007-253C>A	ENSP00000433138.1:n.1007-253C>A
ENST00000534497.5:c.584-253C>A	ENSP00000436875.1:n.584-253C>A
NM_001223.4:c.944-253C>A	NP_001214.1:n.944-253C>A
NM_001257118.2:c.1007-253C>A	NP_001244047.1:n.1007-253C>A
NM_001257119.2:c.944-253C>A	NP_001244048.1:n.944-253C>A
NM_033292.3:c.1007-253C>A	NP_150634.1:n.1007-253C>A
NM_033293.3:c.728-253C>A	NP_150635.1:n.728-253C>A
NM_033294.3:c.584-253C>A	NP_150636.1:n.584-253C>A
NM_033295.3:c.59-253C>A	NP_150637.1:n.59-253C>A
XM_006718924.2:c.1139-253C>A	XP_006718987.2:n.1139-253C>A
XM_011543017.1:c.1139-253C>A	XP_011541319.1:n.1139-253C>A
XM_011543018.1:c.1076-253C>A	XP_011541320.1:n.1076-253C>A
XM_017018393.1:c.998-253C>A	XP_016873882.1:n.998-253C>A
XM_017018394.1:c.998-253C>A	XP_016873883.1:n.998-253C>A
XM_017018395.1:c.935-253C>A	XP_016873884.1:n.935-253C>A
XM_017018396.1:c.917-253C>A	XP_016873885.1:n.917-253C>A
NM_001257118.3:c.1007-253C>A MANE Select	NP_001244047.1:n.1007-253C>A
NM_001223.5:c.944-253C>A	NP_001214.1:n.944-253C>A
NM_001257119.3:c.944-253C>A	NP_001244048.1:n.944-253C>A
NM_033292.4:c.1007-253C>A	NP_150634.1:n.1007-253C>A
NM_033293.4:c.728-253C>A	NP_150635.1:n.728-253C>A
NM_033294.4:c.584-253C>A	NP_150636.1:n.584-253C>A
NM_033295.4:c.59-253C>A	NP_150637.1:n.59-253C>A