Canonical Allele Identifier: CA1619136390
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402560G= , CM000668.2:g.31402560G= GRCh38
NC_000006.11:g.31370337G= , CM000668.1:g.31370337G= GRCh37
NC_000006.10:g.31478316G= NCBI36
NG_034139.1:g.7777G=

Transcript Alleles

HGVS Amino-acid change
ENST00000667609.1:n.468G=
ENST00000673647.1:c.-189+204G= ENSP00000500967.1:n.-189+204G=
ENST00000673996.1:n.79+1777G=
ENST00000674069.1:c.-173+1797G= ENSP00000501157.1:n.-173+1797G=
ENST00000674131.1:c.-189+204G= ENSP00000501002.1:n.-189+204G=
ENST00000616296.4:c.-222+1777G= ENSP00000482382.1:n.-222+1777G=
NM_001289152.1:c.-222+1777G= NP_001276081.1:n.-222+1777G=
NM_001289153.1:c.-222+1797G= NP_001276082.1:n.-222+1797G=
NM_001289154.1:c.-173+1797G= NP_001276083.1:n.-173+1797G=
NM_001289152.2:c.-222+1777G= NP_001276081.1:n.-222+1777G=
NM_001289153.2:c.-222+1797G= NP_001276082.1:n.-222+1797G=
NM_001289154.2:c.-173+1797G= NP_001276083.1:n.-173+1797G=