Canonical Allele Identifier: CA1619136553

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402950_31402951delinsAG , CM000668.2:g.31402950_31402951delinsAG	GRCh38
NC_000006.11:g.31370727_31370728delinsAG , CM000668.1:g.31370727_31370728delinsAG	GRCh37
NC_000006.10:g.31478706_31478707delinsAG	NCBI36
NG_034139.1:g.8167_8168delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.858_859delinsAG
ENST00000673647.1:c.-188-495_-188-494delinsAG	ENSP00000500967.1:n.-188-495_-188-494delinsAG
ENST00000673996.1:n.79+2167_79+2168delinsAG
ENST00000674069.1:c.-173+2187_-173+2188delinsAG	ENSP00000501157.1:n.-173+2187_-173+2188delinsAG
ENST00000674131.1:c.-188-495_-188-494delinsAG	ENSP00000501002.1:n.-188-495_-188-494delinsAG
ENST00000616296.4:c.-222+2167_-222+2168delinsAG	ENSP00000482382.1:n.-222+2167_-222+2168delinsAG
NM_001289152.1:c.-222+2167_-222+2168delinsAG	NP_001276081.1:n.-222+2167_-222+2168delinsAG
NM_001289153.1:c.-222+2187_-222+2188delinsAG	NP_001276082.1:n.-222+2187_-222+2188delinsAG
NM_001289154.1:c.-173+2187_-173+2188delinsAG	NP_001276083.1:n.-173+2187_-173+2188delinsAG
NM_001289152.2:c.-222+2167_-222+2168delinsAG	NP_001276081.1:n.-222+2167_-222+2168delinsAG
NM_001289153.2:c.-222+2187_-222+2188delinsAG	NP_001276082.1:n.-222+2187_-222+2188delinsAG
NM_001289154.2:c.-173+2187_-173+2188delinsAG	NP_001276083.1:n.-173+2187_-173+2188delinsAG