Canonical Allele Identifier: CA2410906316

Linked Data

dbSNP Id: rs2069239332

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50524451_50524457del , CM000684.2:g.50524451_50524457del GRCh38
NC_000022.10:g.50962880_50962886del , CM000684.1:g.50962880_50962886del GRCh37
NC_000022.9:g.49309746_49309752del NCBI36
NG_011860.1:g.10631_10637del , LRG_727:g.10631_10637del
NG_016235.1:g.6985_6991del
NG_021419.1:g.21236_21242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395693.8:c.-13-31_-13-25del (SCO2) MANE Select ENSP00000379046.4:n.-13-31_-13-25del
ENST00000420993.7:c.*1076_*1082del (NCAPH2) MANE Select ENSP00000410088.2:n.*1076_*1082del
ENST00000543927.6:c.-13-31_-13-25del (SCO2) ENSP00000444433.1:n.-13-31_-13-25del
ENST00000638598.2:c.-13-31_-13-25del (SCO2) ENSP00000491753.2:n.-13-31_-13-25del
ENST00000252785.3:c.-13-31_-13-25del ENSP00000252785.3:n.-13-31_-13-25del
ENST00000395693.7:c.-13-31_-13-25del ENSP00000379046.3:n.-13-31_-13-25del
ENST00000423348.1:c.-13-31_-13-25del ENSP00000403570.1:n.-13-31_-13-25del
ENST00000439934.5:c.-13-31_-13-25del ENSP00000415642.1:n.-13-31_-13-25del
ENST00000535425.5:c.-13-31_-13-25del ENSP00000444242.1:n.-13-31_-13-25del
ENST00000543927.5:c.-13-31_-13-25del ENSP00000444433.1:n.-13-31_-13-25del
NM_001169109.1:c.-13-31_-13-25del (SCO2) NP_001162580.1:n.-13-31_-13-25del
NM_001169110.1:c.-13-31_-13-25del (SCO2) NP_001162581.1:n.-13-31_-13-25del
NM_001169111.1:c.-13-31_-13-25del (SCO2) NP_001162582.1:n.-13-31_-13-25del
NM_001185011.1:c.*1076_*1082del (NCAPH2) NP_001171940.1:n.*1076_*1082del
NM_005138.2:c.-13-31_-13-25del (SCO2) NP_005129.2:n.-13-31_-13-25del
NM_152299.3:c.*1076_*1082del (NCAPH2) NP_689512.2:n.*1076_*1082del
XR_001755232.1:n.3104_3110del (NCAPH2)
NM_152299.4:c.*1076_*1082del (NCAPH2) MANE Select NP_689512.2:n.*1076_*1082del
NM_001185011.2:c.*1076_*1082del (NCAPH2) NP_001171940.1:n.*1076_*1082del
NM_005138.3:c.-13-31_-13-25del (SCO2) MANE Select NP_005129.2:n.-13-31_-13-25del
NM_001169109.2:c.-13-31_-13-25del (SCO2) NP_001162580.1:n.-13-31_-13-25del
NM_001169111.2:c.-13-31_-13-25del (SCO2) NP_001162582.1:n.-13-31_-13-25del