Canonical Allele Identifier: CA2371370112
Community Standard Title: NM_020356.4(CASS4):c.460-2696T=
Gene: CASS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.56443204T= , CM000682.2:g.56443204T= GRCh38
NC_000020.10:g.55018260T= , CM000682.1:g.55018260T= GRCh37
NC_000020.9:g.54451667T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020356.4:c.460-2696T= MANE Select NP_065089.2:n.460-2696T=
ENST00000679887.1:c.460-2696T= MANE Select ENSP00000506506.1:n.460-2696T=
NM_001164114.1:c.298-2696T= NP_001157586.1:n.298-2696T=
NM_001164114.2:c.298-2696T= NP_001157586.1:n.298-2696T=
NM_001164115.1:c.460-2696T= NP_001157587.1:n.460-2696T=
NM_001164115.2:c.460-2696T= NP_001157587.1:n.460-2696T=
NM_001164116.1:c.460-2696T= NP_001157588.1:n.460-2696T=
NM_001164116.2:c.460-2696T= NP_001157588.1:n.460-2696T=
NM_020356.3:c.460-2696T= NP_065089.2:n.460-2696T=
ENST00000360314.7:c.460-2696T= ENSP00000353462.3:n.460-2696T=
ENST00000434344.2:c.460-2696T= ENSP00000410027.1:n.460-2696T=
ENST00000497244.1:n.611-2696T=
ENST00000679529.1:c.298-2696T= ENSP00000505834.1:n.298-2696T=
XM_006723831.2:c.298-2696T= XP_006723894.1:n.298-2696T=
XM_006723831.3:c.298-2696T= XP_006723894.1:n.298-2696T=