Canonical Allele Identifier: CA515387172

Linked Data

ClinVar Variation Id: 2860330
ClinVar RCV Id: RCV003696797
dbSNP Id: rs1345472396

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50524055G>A , CM000684.2:g.50524055G>A GRCh38
NC_000022.10:g.50962484G>A , CM000684.1:g.50962484G>A GRCh37
NC_000022.9:g.49309350G>A NCBI36
NG_011860.1:g.11031C>T , LRG_727:g.11031C>T
NG_016235.1:g.7385C>T
NG_021419.1:g.20840G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395693.8:c.357C>T (SCO2) MANE Select ENSP00000379046.4:p.Phe119=
ENST00000420993.7:c.*680G>A (NCAPH2) MANE Select ENSP00000410088.2:n.*680G>A
ENST00000543927.6:c.357C>T (SCO2) ENSP00000444433.1:p.Phe119=
ENST00000638598.2:c.357C>T (SCO2) ENSP00000491753.2:p.Phe119=
ENST00000252785.3:c.357C>T ENSP00000252785.3:p.Phe119=
ENST00000395693.7:c.357C>T ENSP00000379046.3:p.Phe119=
ENST00000423348.1:c.357C>T ENSP00000403570.1:p.Phe119=
ENST00000439934.5:c.357C>T ENSP00000415642.1:p.Phe119=
ENST00000535425.5:c.357C>T ENSP00000444242.1:p.Phe119=
ENST00000543927.5:c.357C>T ENSP00000444433.1:p.Phe119=
NM_001169109.1:c.357C>T (SCO2) NP_001162580.1:p.Phe119=
NM_001169110.1:c.357C>T (SCO2) NP_001162581.1:p.Phe119=
NM_001169111.1:c.357C>T (SCO2) NP_001162582.1:p.Phe119=
NM_001185011.1:c.*680G>A (NCAPH2) NP_001171940.1:n.*680G>A
NM_005138.2:c.357C>T (SCO2) NP_005129.2:p.Phe119=
NM_152299.3:c.*680G>A (NCAPH2) NP_689512.2:n.*680G>A
XR_001755232.1:n.2708G>A (NCAPH2)
NM_152299.4:c.*680G>A (NCAPH2) MANE Select NP_689512.2:n.*680G>A
NM_001185011.2:c.*680G>A (NCAPH2) NP_001171940.1:n.*680G>A
NM_005138.3:c.357C>T (SCO2) MANE Select NP_005129.2:p.Phe119=
NM_001169109.2:c.357C>T (SCO2) NP_001162580.1:p.Phe119=
NM_001169111.2:c.357C>T (SCO2) NP_001162582.1:p.Phe119=