Canonical Allele Identifier: CA1619136388
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402557T= , CM000668.2:g.31402557T= GRCh38
NC_000006.11:g.31370334T= , CM000668.1:g.31370334T= GRCh37
NC_000006.10:g.31478313T= NCBI36
NG_034139.1:g.7774T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.465T=
ENST00000673647.1:c.-189+201T= ENSP00000500967.1:n.-189+201T=
ENST00000673996.1:n.79+1774T=
ENST00000674069.1:c.-173+1794T= ENSP00000501157.1:n.-173+1794T=
ENST00000674131.1:c.-189+201T= ENSP00000501002.1:n.-189+201T=
ENST00000616296.4:c.-222+1774T= ENSP00000482382.1:n.-222+1774T=
NM_001289152.1:c.-222+1774T= NP_001276081.1:n.-222+1774T=
NM_001289153.1:c.-222+1794T= NP_001276082.1:n.-222+1794T=
NM_001289154.1:c.-173+1794T= NP_001276083.1:n.-173+1794T=
NM_001289152.2:c.-222+1774T= NP_001276081.1:n.-222+1774T=
NM_001289153.2:c.-222+1794T= NP_001276082.1:n.-222+1794T=
NM_001289154.2:c.-173+1794T= NP_001276083.1:n.-173+1794T=