Canonical Allele Identifier: CA1484723300
Gene: CASP6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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