Canonical Allele Identifier: CA1619136338

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402450_31402451delinsAG , CM000668.2:g.31402450_31402451delinsAG	GRCh38
NC_000006.11:g.31370227_31370228delinsAG , CM000668.1:g.31370227_31370228delinsAG	GRCh37
NC_000006.10:g.31478206_31478207delinsAG	NCBI36
NG_034139.1:g.7667_7668delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.358_359delinsAG
ENST00000673647.1:c.-189+94_-189+95delinsAG	ENSP00000500967.1:n.-189+94_-189+95delinsAG
ENST00000673996.1:n.79+1667_79+1668delinsAG
ENST00000674069.1:c.-173+1687_-173+1688delinsAG	ENSP00000501157.1:n.-173+1687_-173+1688delinsAG
ENST00000674131.1:c.-189+94_-189+95delinsAG	ENSP00000501002.1:n.-189+94_-189+95delinsAG
ENST00000616296.4:c.-222+1667_-222+1668delinsAG	ENSP00000482382.1:n.-222+1667_-222+1668delinsAG
NM_001289152.1:c.-222+1667_-222+1668delinsAG	NP_001276081.1:n.-222+1667_-222+1668delinsAG
NM_001289153.1:c.-222+1687_-222+1688delinsAG	NP_001276082.1:n.-222+1687_-222+1688delinsAG
NM_001289154.1:c.-173+1687_-173+1688delinsAG	NP_001276083.1:n.-173+1687_-173+1688delinsAG
NM_001289152.2:c.-222+1667_-222+1668delinsAG	NP_001276081.1:n.-222+1667_-222+1668delinsAG
NM_001289153.2:c.-222+1687_-222+1688delinsAG	NP_001276082.1:n.-222+1687_-222+1688delinsAG
NM_001289154.2:c.-173+1687_-173+1688delinsAG	NP_001276083.1:n.-173+1687_-173+1688delinsAG