Canonical Allele Identifier: CA1619136419

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402630_31402632delinsAAT , CM000668.2:g.31402630_31402632delinsAAT	GRCh38
NC_000006.11:g.31370407_31370409delinsAAT , CM000668.1:g.31370407_31370409delinsAAT	GRCh37
NC_000006.10:g.31478386_31478388delinsAAT	NCBI36
NG_034139.1:g.7847_7849delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.538_540delinsAAT
ENST00000673647.1:c.-189+274_-189+276delinsAAT	ENSP00000500967.1:n.-189+274_-189+276delinsAAT
ENST00000673996.1:n.79+1847_79+1849delinsAAT
ENST00000674069.1:c.-173+1867_-173+1869delinsAAT	ENSP00000501157.1:n.-173+1867_-173+1869delinsAAT
ENST00000674131.1:c.-189+274_-189+276delinsAAT	ENSP00000501002.1:n.-189+274_-189+276delinsAAT
ENST00000616296.4:c.-222+1847_-222+1849delinsAAT	ENSP00000482382.1:n.-222+1847_-222+1849delinsAAT
NM_001289152.1:c.-222+1847_-222+1849delinsAAT	NP_001276081.1:n.-222+1847_-222+1849delinsAAT
NM_001289153.1:c.-222+1867_-222+1869delinsAAT	NP_001276082.1:n.-222+1867_-222+1869delinsAAT
NM_001289154.1:c.-173+1867_-173+1869delinsAAT	NP_001276083.1:n.-173+1867_-173+1869delinsAAT
NM_001289152.2:c.-222+1847_-222+1849delinsAAT	NP_001276081.1:n.-222+1847_-222+1849delinsAAT
NM_001289153.2:c.-222+1867_-222+1869delinsAAT	NP_001276082.1:n.-222+1867_-222+1869delinsAAT
NM_001289154.2:c.-173+1867_-173+1869delinsAAT	NP_001276083.1:n.-173+1867_-173+1869delinsAAT