Canonical Allele Identifier: CA2677962465

Gene: MICA

Linked Data

• gnomAD v4: 6-31402271-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402275_31402276del , CM000668.2:g.31402275_31402276del	GRCh38
NC_000006.11:g.31370052_31370053del , CM000668.1:g.31370052_31370053del	GRCh37
NC_000006.10:g.31478031_31478032del	NCBI36
NG_034139.1:g.7492_7493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.183_184del
ENST00000673647.1:c.-270_-269del	ENSP00000500967.1:n.-270_-269del
ENST00000673996.1:n.79+1492_79+1493del
ENST00000674069.1:c.-173+1512_-173+1513del	ENSP00000501157.1:n.-173+1512_-173+1513del
ENST00000674131.1:c.-270_-269del	ENSP00000501002.1:n.-270_-269del
ENST00000616296.4:c.-222+1492_-222+1493del	ENSP00000482382.1:n.-222+1492_-222+1493del
NM_001289152.1:c.-222+1492_-222+1493del	NP_001276081.1:n.-222+1492_-222+1493del
NM_001289153.1:c.-222+1512_-222+1513del	NP_001276082.1:n.-222+1512_-222+1513del
NM_001289154.1:c.-173+1512_-173+1513del	NP_001276083.1:n.-173+1512_-173+1513del
NM_001289152.2:c.-222+1492_-222+1493del	NP_001276081.1:n.-222+1492_-222+1493del
NM_001289153.2:c.-222+1512_-222+1513del	NP_001276082.1:n.-222+1512_-222+1513del
NM_001289154.2:c.-173+1512_-173+1513del	NP_001276083.1:n.-173+1512_-173+1513del