Canonical Allele Identifier: CA449642846

Gene: MICA

Linked Data

• gnomAD v4: 6-31400756-C-A
• MyVariant Identifiers: chr6:g.31368533C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400756C>A , CM000668.2:g.31400756C>A	GRCh38
NC_000006.11:g.31368533C>A , CM000668.1:g.31368533C>A	GRCh37
NC_000006.10:g.31476512C>A	NCBI36
NG_034139.1:g.5973C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.57C>A
ENST00000673647.1:c.-396C>A	ENSP00000500967.1:n.-396C>A
ENST00000673996.1:n.52C>A
ENST00000674069.1:c.-180C>A	ENSP00000501157.1:n.-180C>A
ENST00000674131.1:c.-416C>A	ENSP00000501002.1:n.-416C>A
ENST00000616296.4:c.-249C>A	ENSP00000482382.1:n.-249C>A
NM_001289152.1:c.-249C>A	NP_001276081.1:n.-249C>A
NM_001289153.1:c.-229C>A	NP_001276082.1:n.-229C>A
NM_001289154.1:c.-180C>A	NP_001276083.1:n.-180C>A
NM_001289152.2:c.-249C>A	NP_001276081.1:n.-249C>A
NM_001289153.2:c.-229C>A	NP_001276082.1:n.-229C>A
NM_001289154.2:c.-180C>A	NP_001276083.1:n.-180C>A