Canonical Allele Identifier: CA2677962020

Gene: MICA

Linked Data

• gnomAD v4: 6-31400767-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400767A>C , CM000668.2:g.31400767A>C	GRCh38
NC_000006.11:g.31368544A>C , CM000668.1:g.31368544A>C	GRCh37
NC_000006.10:g.31476523A>C	NCBI36
NG_034139.1:g.5984A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.64+4A>C
ENST00000673647.1:c.-389+4A>C	ENSP00000500967.1:n.-389+4A>C
ENST00000673996.1:n.63A>C
ENST00000674069.1:c.-173+4A>C	ENSP00000501157.1:n.-173+4A>C
ENST00000674131.1:c.-405A>C	ENSP00000501002.1:n.-405A>C
ENST00000616296.4:c.-238A>C	ENSP00000482382.1:n.-238A>C
NM_001289152.1:c.-238A>C	NP_001276081.1:n.-238A>C
NM_001289153.1:c.-222+4A>C	NP_001276082.1:n.-222+4A>C
NM_001289154.1:c.-173+4A>C	NP_001276083.1:n.-173+4A>C
NM_001289152.2:c.-238A>C	NP_001276081.1:n.-238A>C
NM_001289153.2:c.-222+4A>C	NP_001276082.1:n.-222+4A>C
NM_001289154.2:c.-173+4A>C	NP_001276083.1:n.-173+4A>C