Canonical Allele Identifier: CA2194749621

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89624877C= , CM000677.2:g.89624877C= GRCh38
NC_000015.9:g.90168108C= , CM000677.1:g.90168108C= GRCh37
NC_000015.8:g.87969112C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268138.12:c.4567C= (TICRR) MANE Select ENSP00000268138.7:p.Arg1523=
ENST00000268138.11:c.4567C= (TICRR) ENSP00000268138.7:p.Arg1523=
ENST00000558928.1:n.180+3724G= (KIF7)
ENST00000560985.5:c.4564C= (TICRR) ENSP00000453306.1:p.Arg1522=
NM_001308025.1:c.4564C= (TICRR) NP_001294954.1:p.Arg1522=
NM_152259.3:c.4567C= (TICRR) NP_689472.3:p.Arg1523=
XM_011521534.1:c.3973+3724G= (KIF7) XP_011519836.1:n.3973+3724G=
XM_011521535.1:c.3973+3724G= (KIF7) XP_011519837.1:n.3973+3724G=
XM_011521536.1:c.3973+3724G= (KIF7) XP_011519838.1:n.3973+3724G=
XM_011522162.1:c.4567C= (TICRR) XP_011520464.1:p.Arg1523=
NM_152259.4:c.4567C= (TICRR) MANE Select NP_689472.3:p.Arg1523=