Canonical Allele Identifier: CA1619136421
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402633A= , CM000668.2:g.31402633A= GRCh38
NC_000006.11:g.31370410A= , CM000668.1:g.31370410A= GRCh37
NC_000006.10:g.31478389A= NCBI36
NG_034139.1:g.7850A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.541A=
ENST00000673647.1:c.-189+277A= ENSP00000500967.1:n.-189+277A=
ENST00000673996.1:n.79+1850A=
ENST00000674069.1:c.-173+1870A= ENSP00000501157.1:n.-173+1870A=
ENST00000674131.1:c.-189+277A= ENSP00000501002.1:n.-189+277A=
ENST00000616296.4:c.-222+1850A= ENSP00000482382.1:n.-222+1850A=
NM_001289152.1:c.-222+1850A= NP_001276081.1:n.-222+1850A=
NM_001289153.1:c.-222+1870A= NP_001276082.1:n.-222+1870A=
NM_001289154.1:c.-173+1870A= NP_001276083.1:n.-173+1870A=
NM_001289152.2:c.-222+1850A= NP_001276081.1:n.-222+1850A=
NM_001289153.2:c.-222+1870A= NP_001276082.1:n.-222+1870A=
NM_001289154.2:c.-173+1870A= NP_001276083.1:n.-173+1870A=