Canonical Allele Identifier: CA1667372412
Gene: CITED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373445G= , CM000668.2:g.139373445G= GRCh38
NC_000006.11:g.139694582G= , CM000668.1:g.139694582G= GRCh37
NC_000006.10:g.139736275G= NCBI36
NG_016169.1:g.6204C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.500C= MANE Select ENSP00000356623.2:p.Pro167=
ENST00000367651.3:c.500C= ENSP00000356623.2:p.Pro167=
ENST00000536159.2:c.500C= ENSP00000442831.1:p.Pro167=
ENST00000537332.2:c.515C= ENSP00000444198.2:p.Pro172=
ENST00000618718.1:c.476+24C= ENSP00000479918.1:n.476+24C=
NM_001168388.2:c.500C= NP_001161860.1:p.Pro167=
NM_001168389.2:c.515C= NP_001161861.2:p.Pro172=
NM_006079.4:c.500C= NP_006070.2:p.Pro167=
NM_006079.5:c.500C= MANE Select NP_006070.2:p.Pro167=
NM_001168388.3:c.500C= NP_001161860.1:p.Pro167=
NM_001168389.3:c.515C= NP_001161861.2:p.Pro172=