Canonical Allele Identifier: CA1619140120

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31411332G= , CM000668.2:g.31411332G=	GRCh38
NC_000006.11:g.31379109G= , CM000668.1:g.31379109G=	GRCh37
NC_000006.10:g.31487088G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001177519.3:c.586G= MANE Select	NP_001170990.1:p.Glu196=
ENST00000449934.7:c.586G= MANE Select	ENSP00000413079.1:p.Glu196=
NM_001177519.2:c.586G=	NP_001170990.1:p.Glu196=
NM_001289152.1:c.295G=	NP_001276081.1:p.Glu99=
NM_001289152.2:c.295G=	NP_001276081.1:p.Glu99=
NM_001289153.1:c.295G=	NP_001276082.1:p.Glu99=
NM_001289153.2:c.295G=	NP_001276082.1:p.Glu99=
NM_001289154.1:c.172G=	NP_001276083.1:p.Glu58=
NM_001289154.2:c.172G=	NP_001276083.1:p.Glu58=
ENST00000421350.1:c.286+535G=	ENSP00000402410.1:n.286+535G=
ENST00000449934.6:c.586G=	ENSP00000413079.1:p.Glu196=
ENST00000616296.4:c.295G=	ENSP00000482382.1:p.Glu99=
ENST00000673996.1:n.595G=
ENST00000674069.1:c.172G=	ENSP00000501157.1:p.Glu58=