Canonical Allele Identifier: CA2513791994
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402524G>A , CM000668.2:g.31402524G>A GRCh38
NC_000006.11:g.31370301G>A , CM000668.1:g.31370301G>A GRCh37
NC_000006.10:g.31478280G>A NCBI36
NG_034139.1:g.7741G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000667609.1:n.432G>A
ENST00000673647.1:c.-189+168G>A ENSP00000500967.1:n.-189+168G>A
ENST00000673996.1:n.79+1741G>A
ENST00000674069.1:c.-173+1761G>A ENSP00000501157.1:n.-173+1761G>A
ENST00000674131.1:c.-189+168G>A ENSP00000501002.1:n.-189+168G>A
ENST00000616296.4:c.-222+1741G>A ENSP00000482382.1:n.-222+1741G>A
NM_001289152.1:c.-222+1741G>A NP_001276081.1:n.-222+1741G>A
NM_001289153.1:c.-222+1761G>A NP_001276082.1:n.-222+1761G>A
NM_001289154.1:c.-173+1761G>A NP_001276083.1:n.-173+1761G>A
NM_001289152.2:c.-222+1741G>A NP_001276081.1:n.-222+1741G>A
NM_001289153.2:c.-222+1761G>A NP_001276082.1:n.-222+1761G>A
NM_001289154.2:c.-173+1761G>A NP_001276083.1:n.-173+1761G>A