Canonical Allele Identifier: CA1619135689
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31400765T= , CM000668.2:g.31400765T= GRCh38
NC_000006.11:g.31368542T= , CM000668.1:g.31368542T= GRCh37
NC_000006.10:g.31476521T= NCBI36
NG_034139.1:g.5982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.64+2T=
ENST00000673647.1:c.-389+2T= ENSP00000500967.1:n.-389+2T=
ENST00000673996.1:n.61T=
ENST00000674069.1:c.-173+2T= ENSP00000501157.1:n.-173+2T=
ENST00000674131.1:c.-407T= ENSP00000501002.1:n.-407T=
ENST00000616296.4:c.-240T= ENSP00000482382.1:n.-240T=
NM_001289152.1:c.-240T= NP_001276081.1:n.-240T=
NM_001289153.1:c.-222+2T= NP_001276082.1:n.-222+2T=
NM_001289154.1:c.-173+2T= NP_001276083.1:n.-173+2T=
NM_001289152.2:c.-240T= NP_001276081.1:n.-240T=
NM_001289153.2:c.-222+2T= NP_001276082.1:n.-222+2T=
NM_001289154.2:c.-173+2T= NP_001276083.1:n.-173+2T=