Canonical Allele Identifier: CA136862500

Gene: MICA

Linked Data

• dbSNP Id: rs34771872
• MyVariant Identifiers: chr6:g.31370050_31370051insG (hg19) ; chr6:g.31402273_31402274insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402274dup , CM000668.2:g.31402274dup	GRCh38
NC_000006.11:g.31370051dup , CM000668.1:g.31370051dup	GRCh37
NC_000006.10:g.31478030dup	NCBI36
NG_034139.1:g.7491dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.182dup
ENST00000673647.1:c.-271dup	ENSP00000500967.1:n.-271dup
ENST00000673996.1:n.79+1491dup
ENST00000674069.1:c.-173+1511dup	ENSP00000501157.1:n.-173+1511dup
ENST00000674131.1:c.-271dup	ENSP00000501002.1:n.-271dup
ENST00000616296.4:c.-222+1491dup	ENSP00000482382.1:n.-222+1491dup
NM_001289152.1:c.-222+1491dup	NP_001276081.1:n.-222+1491dup
NM_001289153.1:c.-222+1511dup	NP_001276082.1:n.-222+1511dup
NM_001289154.1:c.-173+1511dup	NP_001276083.1:n.-173+1511dup
NM_001289152.2:c.-222+1491dup	NP_001276081.1:n.-222+1491dup
NM_001289153.2:c.-222+1511dup	NP_001276082.1:n.-222+1511dup
NM_001289154.2:c.-173+1511dup	NP_001276083.1:n.-173+1511dup