Canonical Allele Identifier: CA3712243

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31412154G>A , CM000668.2:g.31412154G>A	GRCh38
NC_000006.11:g.31379931G>A , CM000668.1:g.31379931G>A	GRCh37
NC_000006.10:g.31487910G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449934.7:c.821G>A MANE Select	ENSP00000413079.1:p.Arg274Gln
ENST00000674069.1:c.407G>A	ENSP00000501157.1:p.Arg136Gln
ENST00000421350.1:c.494G>A	ENSP00000402410.1:p.Arg165Gln
ENST00000449934.6:c.821G>A	ENSP00000413079.1:p.Arg274Gln
ENST00000616296.4:c.530G>A	ENSP00000482382.1:p.Arg177Gln
NM_001177519.2:c.821G>A	NP_001170990.1:p.Arg274Gln
NM_001289152.1:c.530G>A	NP_001276081.1:p.Arg177Gln
NM_001289153.1:c.530G>A	NP_001276082.1:p.Arg177Gln
NM_001289154.1:c.407G>A	NP_001276083.1:p.Arg136Gln
NM_001177519.3:c.821G>A MANE Select	NP_001170990.1:p.Arg274Gln
NM_001289152.2:c.530G>A	NP_001276081.1:p.Arg177Gln
NM_001289153.2:c.530G>A	NP_001276082.1:p.Arg177Gln
NM_001289154.2:c.407G>A	NP_001276083.1:p.Arg136Gln