Canonical Allele Identifier: CA1619136310

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402384_31402385delinsCT , CM000668.2:g.31402384_31402385delinsCT	GRCh38
NC_000006.11:g.31370161_31370162delinsCT , CM000668.1:g.31370161_31370162delinsCT	GRCh37
NC_000006.10:g.31478140_31478141delinsCT	NCBI36
NG_034139.1:g.7601_7602delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.292_293delinsCT
ENST00000673647.1:c.-189+28_-189+29delinsCT	ENSP00000500967.1:n.-189+28_-189+29delinsCT
ENST00000673996.1:n.79+1601_79+1602delinsCT
ENST00000674069.1:c.-173+1621_-173+1622delinsCT	ENSP00000501157.1:n.-173+1621_-173+1622delinsCT
ENST00000674131.1:c.-189+28_-189+29delinsCT	ENSP00000501002.1:n.-189+28_-189+29delinsCT
ENST00000616296.4:c.-222+1601_-222+1602delinsCT	ENSP00000482382.1:n.-222+1601_-222+1602delinsCT
NM_001289152.1:c.-222+1601_-222+1602delinsCT	NP_001276081.1:n.-222+1601_-222+1602delinsCT
NM_001289153.1:c.-222+1621_-222+1622delinsCT	NP_001276082.1:n.-222+1621_-222+1622delinsCT
NM_001289154.1:c.-173+1621_-173+1622delinsCT	NP_001276083.1:n.-173+1621_-173+1622delinsCT
NM_001289152.2:c.-222+1601_-222+1602delinsCT	NP_001276081.1:n.-222+1601_-222+1602delinsCT
NM_001289153.2:c.-222+1621_-222+1622delinsCT	NP_001276082.1:n.-222+1621_-222+1622delinsCT
NM_001289154.2:c.-173+1621_-173+1622delinsCT	NP_001276083.1:n.-173+1621_-173+1622delinsCT