Canonical Allele Identifier: CA1619140067

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31411200G= , CM000668.2:g.31411200G=	GRCh38
NC_000006.11:g.31378977G= , CM000668.1:g.31378977G=	GRCh37
NC_000006.10:g.31486956G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449934.7:c.454G= MANE Select	ENSP00000413079.1:p.Val152=
ENST00000673996.1:n.463G=
ENST00000674069.1:c.84-44G=	ENSP00000501157.1:n.84-44G=
ENST00000421350.1:c.286+403G=	ENSP00000402410.1:n.286+403G=
ENST00000449934.6:c.454G=	ENSP00000413079.1:p.Val152=
ENST00000616296.4:c.163G=	ENSP00000482382.1:p.Val55=
NM_001177519.2:c.454G=	NP_001170990.1:p.Val152=
NM_001289152.1:c.163G=	NP_001276081.1:p.Val55=
NM_001289153.1:c.163G=	NP_001276082.1:p.Val55=
NM_001289154.1:c.84-44G=	NP_001276083.1:n.84-44G=
NM_001177519.3:c.454G= MANE Select	NP_001170990.1:p.Val152=
NM_001289152.2:c.163G=	NP_001276081.1:p.Val55=
NM_001289153.2:c.163G=	NP_001276082.1:p.Val55=
NM_001289154.2:c.84-44G=	NP_001276083.1:n.84-44G=