Canonical Allele Identifier: CA1619139356

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31409810G= , CM000668.2:g.31409810G=	GRCh38
NC_000006.11:g.31377587G= , CM000668.1:g.31377587G=	GRCh37
NC_000006.10:g.31485566G=	NCBI36
NG_034139.1:g.15130G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449934.7:c.71-733G= MANE Select	ENSP00000413079.1:n.71-733G=
ENST00000673647.1:c.71-733G=	ENSP00000500967.1:n.71-733G=
ENST00000673996.1:n.80-733G=
ENST00000674069.1:c.-172-733G=	ENSP00000501157.1:n.-172-733G=
ENST00000421350.1:c.32-733G=	ENSP00000402410.1:n.32-733G=
ENST00000449934.6:c.71-733G=	ENSP00000413079.1:n.71-733G=
ENST00000616296.4:c.-221-733G=	ENSP00000482382.1:n.-221-733G=
NM_001177519.2:c.71-733G=	NP_001170990.1:n.71-733G=
NM_001289152.1:c.-221-733G=	NP_001276081.1:n.-221-733G=
NM_001289153.1:c.-221-733G=	NP_001276082.1:n.-221-733G=
NM_001289154.1:c.-172-733G=	NP_001276083.1:n.-172-733G=
NM_001177519.3:c.71-733G= MANE Select	NP_001170990.1:n.71-733G=
NM_001289152.2:c.-221-733G=	NP_001276081.1:n.-221-733G=
NM_001289153.2:c.-221-733G=	NP_001276082.1:n.-221-733G=
NM_001289154.2:c.-172-733G=	NP_001276083.1:n.-172-733G=