Canonical Allele Identifier: CA15446386

Gene: MICA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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