Canonical Allele Identifier: CA1484723299

Gene: CASP6

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109698378T= , CM000666.2:g.109698378T=	GRCh38
NC_000004.11:g.110619534T= , CM000666.1:g.110619534T=	GRCh37
NC_000004.10:g.110838983T=	NCBI36
NG_029187.1:g.10096A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001226.4:c.41-36A= MANE Select	NP_001217.2:n.41-36A=
ENST00000265164.7:c.41-36A= MANE Select	ENSP00000265164.2:n.41-36A=
NM_001226.3:c.41-36A=	NP_001217.2:n.41-36A=
NM_032992.2:c.41-3678A=	NP_116787.1:n.41-3678A=
NM_032992.3:c.41-3678A=	NP_116787.1:n.41-3678A=
NR_133012.1:n.119-36A=
NR_133012.2:n.91-36A=
ENST00000265164.6:c.41-36A=	ENSP00000265164.2:n.41-36A=
ENST00000352981.7:c.41-3678A=	ENSP00000285333.3:n.41-3678A=
ENST00000503684.5:c.-14-36A=	ENSP00000427669.1:n.-14-36A=
ENST00000505486.1:c.41-36A=	ENSP00000424080.1:n.41-36A=
XM_005263271.3:c.17-36A=	XP_005263328.1:n.17-36A=