Canonical Allele Identifier: CA2677962133

Gene: MICA

Linked Data

• gnomAD v4: 6-31400861-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400861G>A , CM000668.2:g.31400861G>A	GRCh38
NC_000006.11:g.31368638G>A , CM000668.1:g.31368638G>A	GRCh37
NC_000006.10:g.31476617G>A	NCBI36
NG_034139.1:g.6078G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.64+98G>A
ENST00000673647.1:c.-389+98G>A	ENSP00000500967.1:n.-389+98G>A
ENST00000673996.1:n.79+78G>A
ENST00000674069.1:c.-173+98G>A	ENSP00000501157.1:n.-173+98G>A
ENST00000674131.1:c.-389+78G>A	ENSP00000501002.1:n.-389+78G>A
ENST00000616296.4:c.-222+78G>A	ENSP00000482382.1:n.-222+78G>A
NM_001289152.1:c.-222+78G>A	NP_001276081.1:n.-222+78G>A
NM_001289153.1:c.-222+98G>A	NP_001276082.1:n.-222+98G>A
NM_001289154.1:c.-173+98G>A	NP_001276083.1:n.-173+98G>A
NM_001289152.2:c.-222+78G>A	NP_001276081.1:n.-222+78G>A
NM_001289153.2:c.-222+98G>A	NP_001276082.1:n.-222+98G>A
NM_001289154.2:c.-173+98G>A	NP_001276083.1:n.-173+98G>A