Canonical Allele Identifier: CA2677962559

Gene: MICA

Linked Data

• gnomAD v4: 6-31402395-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402395G>C , CM000668.2:g.31402395G>C	GRCh38
NC_000006.11:g.31370172G>C , CM000668.1:g.31370172G>C	GRCh37
NC_000006.10:g.31478151G>C	NCBI36
NG_034139.1:g.7612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.303G>C
ENST00000673647.1:c.-189+39G>C	ENSP00000500967.1:n.-189+39G>C
ENST00000673996.1:n.79+1612G>C
ENST00000674069.1:c.-173+1632G>C	ENSP00000501157.1:n.-173+1632G>C
ENST00000674131.1:c.-189+39G>C	ENSP00000501002.1:n.-189+39G>C
ENST00000616296.4:c.-222+1612G>C	ENSP00000482382.1:n.-222+1612G>C
NM_001289152.1:c.-222+1612G>C	NP_001276081.1:n.-222+1612G>C
NM_001289153.1:c.-222+1632G>C	NP_001276082.1:n.-222+1632G>C
NM_001289154.1:c.-173+1632G>C	NP_001276083.1:n.-173+1632G>C
NM_001289152.2:c.-222+1612G>C	NP_001276081.1:n.-222+1612G>C
NM_001289153.2:c.-222+1632G>C	NP_001276082.1:n.-222+1632G>C
NM_001289154.2:c.-173+1632G>C	NP_001276083.1:n.-173+1632G>C