Canonical Allele Identifier: CA823884452

Gene: MICA

Linked Data

• dbSNP Id: rs1240999021
• gnomAD v3: 6-31402998-AG-A
• gnomAD v4: 6-31402998-AG-A
• MyVariant Identifiers: chr6:g.31370776del (hg19) ; chr6:g.31402999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402999del , CM000668.2:g.31402999del	GRCh38
NC_000006.11:g.31370776del , CM000668.1:g.31370776del	GRCh37
NC_000006.10:g.31478755del	NCBI36
NG_034139.1:g.8216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.907del
ENST00000673647.1:c.-188-446del	ENSP00000500967.1:n.-188-446del
ENST00000673996.1:n.79+2216del
ENST00000674069.1:c.-173+2236del	ENSP00000501157.1:n.-173+2236del
ENST00000674131.1:c.-188-446del	ENSP00000501002.1:n.-188-446del
ENST00000616296.4:c.-222+2216del	ENSP00000482382.1:n.-222+2216del
NM_001289152.1:c.-222+2216del	NP_001276081.1:n.-222+2216del
NM_001289153.1:c.-222+2236del	NP_001276082.1:n.-222+2236del
NM_001289154.1:c.-173+2236del	NP_001276083.1:n.-173+2236del
NM_001289152.2:c.-222+2216del	NP_001276081.1:n.-222+2216del
NM_001289153.2:c.-222+2236del	NP_001276082.1:n.-222+2236del
NM_001289154.2:c.-173+2236del	NP_001276083.1:n.-173+2236del