Canonical Allele Identifier: CA1087457571

Gene: MICA

Linked Data

• dbSNP Id: rs1770515790
• gnomAD v3: 6-31402887-T-TTC
• gnomAD v4: 6-31402887-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402888_31402889insCT , CM000668.2:g.31402888_31402889insCT	GRCh38
NC_000006.11:g.31370665_31370666insCT , CM000668.1:g.31370665_31370666insCT	GRCh37
NC_000006.10:g.31478644_31478645insCT	NCBI36
NG_034139.1:g.8105_8106insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.796_797insCT
ENST00000673647.1:c.-189+532_-189+533insCT	ENSP00000500967.1:n.-189+532_-189+533insCT
ENST00000673996.1:n.79+2105_79+2106insCT
ENST00000674069.1:c.-173+2125_-173+2126insCT	ENSP00000501157.1:n.-173+2125_-173+2126insCT
ENST00000674131.1:c.-189+532_-189+533insCT	ENSP00000501002.1:n.-189+532_-189+533insCT
ENST00000616296.4:c.-222+2105_-222+2106insCT	ENSP00000482382.1:n.-222+2105_-222+2106insCT
NM_001289152.1:c.-222+2105_-222+2106insCT	NP_001276081.1:n.-222+2105_-222+2106insCT
NM_001289153.1:c.-222+2125_-222+2126insCT	NP_001276082.1:n.-222+2125_-222+2126insCT
NM_001289154.1:c.-173+2125_-173+2126insCT	NP_001276083.1:n.-173+2125_-173+2126insCT
NM_001289152.2:c.-222+2105_-222+2106insCT	NP_001276081.1:n.-222+2105_-222+2106insCT
NM_001289153.2:c.-222+2125_-222+2126insCT	NP_001276082.1:n.-222+2125_-222+2126insCT
NM_001289154.2:c.-173+2125_-173+2126insCT	NP_001276083.1:n.-173+2125_-173+2126insCT