Canonical Allele Identifier: CA1619136323
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402415_31402416delinsTG , CM000668.2:g.31402415_31402416delinsTG GRCh38
NC_000006.11:g.31370192_31370193delinsTG , CM000668.1:g.31370192_31370193delinsTG GRCh37
NC_000006.10:g.31478171_31478172delinsTG NCBI36
NG_034139.1:g.7632_7633delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.323_324delinsTG
ENST00000673647.1:c.-189+59_-189+60delinsTG ENSP00000500967.1:n.-189+59_-189+60delinsTG
ENST00000673996.1:n.79+1632_79+1633delinsTG
ENST00000674069.1:c.-173+1652_-173+1653delinsTG ENSP00000501157.1:n.-173+1652_-173+1653delinsTG
ENST00000674131.1:c.-189+59_-189+60delinsTG ENSP00000501002.1:n.-189+59_-189+60delinsTG
ENST00000616296.4:c.-222+1632_-222+1633delinsTG ENSP00000482382.1:n.-222+1632_-222+1633delinsTG
NM_001289152.1:c.-222+1632_-222+1633delinsTG NP_001276081.1:n.-222+1632_-222+1633delinsTG
NM_001289153.1:c.-222+1652_-222+1653delinsTG NP_001276082.1:n.-222+1652_-222+1653delinsTG
NM_001289154.1:c.-173+1652_-173+1653delinsTG NP_001276083.1:n.-173+1652_-173+1653delinsTG
NM_001289152.2:c.-222+1632_-222+1633delinsTG NP_001276081.1:n.-222+1632_-222+1633delinsTG
NM_001289153.2:c.-222+1652_-222+1653delinsTG NP_001276082.1:n.-222+1652_-222+1653delinsTG
NM_001289154.2:c.-173+1652_-173+1653delinsTG NP_001276083.1:n.-173+1652_-173+1653delinsTG