Canonical Allele Identifier: CA1619135688
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31400764G= , CM000668.2:g.31400764G= GRCh38
NC_000006.11:g.31368541G= , CM000668.1:g.31368541G= GRCh37
NC_000006.10:g.31476520G= NCBI36
NG_034139.1:g.5981G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.64+1G=
ENST00000673647.1:c.-389+1G= ENSP00000500967.1:n.-389+1G=
ENST00000673996.1:n.60G=
ENST00000674069.1:c.-173+1G= ENSP00000501157.1:n.-173+1G=
ENST00000674131.1:c.-408G= ENSP00000501002.1:n.-408G=
ENST00000616296.4:c.-241G= ENSP00000482382.1:n.-241G=
NM_001289152.1:c.-241G= NP_001276081.1:n.-241G=
NM_001289153.1:c.-222+1G= NP_001276082.1:n.-222+1G=
NM_001289154.1:c.-173+1G= NP_001276083.1:n.-173+1G=
NM_001289152.2:c.-241G= NP_001276081.1:n.-241G=
NM_001289153.2:c.-222+1G= NP_001276082.1:n.-222+1G=
NM_001289154.2:c.-173+1G= NP_001276083.1:n.-173+1G=