Canonical Allele Identifier: CA1619135685
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31400759T= , CM000668.2:g.31400759T= GRCh38
NC_000006.11:g.31368536T= , CM000668.1:g.31368536T= GRCh37
NC_000006.10:g.31476515T= NCBI36
NG_034139.1:g.5976T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.60T=
ENST00000673647.1:c.-393T= ENSP00000500967.1:n.-393T=
ENST00000673996.1:n.55T=
ENST00000674069.1:c.-177T= ENSP00000501157.1:n.-177T=
ENST00000674131.1:c.-413T= ENSP00000501002.1:n.-413T=
ENST00000616296.4:c.-246T= ENSP00000482382.1:n.-246T=
NM_001289152.1:c.-246T= NP_001276081.1:n.-246T=
NM_001289153.1:c.-226T= NP_001276082.1:n.-226T=
NM_001289154.1:c.-177T= NP_001276083.1:n.-177T=
NM_001289152.2:c.-246T= NP_001276081.1:n.-246T=
NM_001289153.2:c.-226T= NP_001276082.1:n.-226T=
NM_001289154.2:c.-177T= NP_001276083.1:n.-177T=