Canonical Allele Identifier: CA382271173

Gene: CASP4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.104954939C>T , CM000673.2:g.104954939C>T	GRCh38
NC_000011.9:g.104825666C>T , CM000673.1:g.104825666C>T	GRCh37
NC_000011.8:g.104330876C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001225.4:c.70G>A MANE Select	NP_001216.1:p.Gly24Ser
ENST00000444739.7:c.70G>A MANE Select	ENSP00000388566.2:p.Gly24Ser
NM_001225.3:c.70G>A	NP_001216.1:p.Gly24Ser
NM_033306.2:c.-99G>A	NP_150649.1:n.-99G>A
NM_033306.3:c.-99G>A	NP_150649.1:n.-99G>A
ENST00000393150.7:c.-99G>A	ENSP00000376857.3:n.-99G>A
ENST00000417440.2:c.70G>A	ENSP00000401673.2:p.Gly24Ser
ENST00000444739.6:c.70G>A	ENSP00000388566.2:p.Gly24Ser
ENST00000524843.5:n.126G>A
ENST00000529183.5:n.110G>A
ENST00000531333.5:n.184G>A
ENST00000531546.1:n.120G>A
ENST00000533730.5:n.92G>A
ENST00000613196.4:c.-70G>A	ENSP00000482808.1:n.-70G>A
XM_011543019.1:c.-262G>A	XP_011541321.1:n.-262G>A
XM_017018397.1:c.-262G>A	XP_016873886.1:n.-262G>A