Canonical Allele Identifier: CA1667372123
Gene: CITED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372960_139372963delinsGGCA , CM000668.2:g.139372960_139372963delinsGGCA GRCh38
NC_000006.11:g.139694097_139694100delinsGGCA , CM000668.1:g.139694097_139694100delinsGGCA GRCh37
NC_000006.10:g.139735790_139735793delinsGGCA NCBI36
NG_016169.1:g.6686_6689delinsTGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*169_*172delinsTGCC MANE Select ENSP00000356623.2:n.*169_*172delinsTGCC
ENST00000367651.3:c.*169_*172delinsTGCC ENSP00000356623.2:n.*169_*172delinsTGCC
ENST00000536159.2:c.*169_*172delinsTGCC ENSP00000442831.1:n.*169_*172delinsTGCC
ENST00000537332.2:c.*169_*172delinsTGCC ENSP00000444198.2:n.*169_*172delinsTGCC
NM_001168388.2:c.*169_*172delinsTGCC NP_001161860.1:n.*169_*172delinsTGCC
NM_001168389.2:c.*169_*172delinsTGCC NP_001161861.2:n.*169_*172delinsTGCC
NM_006079.4:c.*169_*172delinsTGCC NP_006070.2:n.*169_*172delinsTGCC
NM_006079.5:c.*169_*172delinsTGCC MANE Select NP_006070.2:n.*169_*172delinsTGCC
NM_001168388.3:c.*169_*172delinsTGCC NP_001161860.1:n.*169_*172delinsTGCC
NM_001168389.3:c.*169_*172delinsTGCC NP_001161861.2:n.*169_*172delinsTGCC