Canonical Allele Identifier: CA1619136446
Gene: MICA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402698_31402704delinsGGATGGT , CM000668.2:g.31402698_31402704delinsGGATGGT GRCh38
NC_000006.11:g.31370475_31370481delinsGGATGGT , CM000668.1:g.31370475_31370481delinsGGATGGT GRCh37
NC_000006.10:g.31478454_31478460delinsGGATGGT NCBI36
NG_034139.1:g.7915_7921delinsGGATGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000667609.1:n.606_612delinsGGATGGT
ENST00000673647.1:c.-189+342_-189+348delinsGGATGGT ENSP00000500967.1:n.-189+342_-189+348delinsGGATGGT
ENST00000673996.1:n.79+1915_79+1921delinsGGATGGT
ENST00000674069.1:c.-173+1935_-173+1941delinsGGATGGT ENSP00000501157.1:n.-173+1935_-173+1941delinsGGATGGT
ENST00000674131.1:c.-189+342_-189+348delinsGGATGGT ENSP00000501002.1:n.-189+342_-189+348delinsGGATGGT
ENST00000616296.4:c.-222+1915_-222+1921delinsGGATGGT ENSP00000482382.1:n.-222+1915_-222+1921delinsGGATGGT
NM_001289152.1:c.-222+1915_-222+1921delinsGGATGGT NP_001276081.1:n.-222+1915_-222+1921delinsGGATGGT
NM_001289153.1:c.-222+1935_-222+1941delinsGGATGGT NP_001276082.1:n.-222+1935_-222+1941delinsGGATGGT
NM_001289154.1:c.-173+1935_-173+1941delinsGGATGGT NP_001276083.1:n.-173+1935_-173+1941delinsGGATGGT
NM_001289152.2:c.-222+1915_-222+1921delinsGGATGGT NP_001276081.1:n.-222+1915_-222+1921delinsGGATGGT
NM_001289153.2:c.-222+1935_-222+1941delinsGGATGGT NP_001276082.1:n.-222+1935_-222+1941delinsGGATGGT
NM_001289154.2:c.-173+1935_-173+1941delinsGGATGGT NP_001276083.1:n.-173+1935_-173+1941delinsGGATGGT