Canonical Allele Identifier: CA823890932

Gene: MICA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31412752A>T , CM000668.2:g.31412752A>T	GRCh38
NC_000006.11:g.31380529A>T , CM000668.1:g.31380529A>T	GRCh37
NC_000006.10:g.31488508A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449934.7:c.*29+292A>T MANE Select	ENSP00000413079.1:n.*29+292A>T
ENST00000674069.1:c.*29+292A>T	ENSP00000501157.1:n.*29+292A>T
ENST00000421350.1:c.701+292A>T	ENSP00000402410.1:n.701+292A>T
ENST00000449934.6:c.*29+292A>T	ENSP00000413079.1:n.*29+292A>T
ENST00000616296.4:c.*29+292A>T	ENSP00000482382.1:n.*29+292A>T
NM_001177519.2:c.*29+292A>T	NP_001170990.1:n.*29+292A>T
NM_001289152.1:c.*29+292A>T	NP_001276081.1:n.*29+292A>T
NM_001289153.1:c.*29+292A>T	NP_001276082.1:n.*29+292A>T
NM_001289154.1:c.*29+292A>T	NP_001276083.1:n.*29+292A>T
NM_001177519.3:c.*29+292A>T MANE Select	NP_001170990.1:n.*29+292A>T
NM_001289152.2:c.*29+292A>T	NP_001276081.1:n.*29+292A>T
NM_001289153.2:c.*29+292A>T	NP_001276082.1:n.*29+292A>T
NM_001289154.2:c.*29+292A>T	NP_001276083.1:n.*29+292A>T