Canonical Allele Identifier: CA2711312751

Gene: MICA

Linked Data

• dbSNP Id: rs2113716221

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402918_31402931del , CM000668.2:g.31402918_31402931del	GRCh38
NC_000006.11:g.31370695_31370708del , CM000668.1:g.31370695_31370708del	GRCh37
NC_000006.10:g.31478674_31478687del	NCBI36
NG_034139.1:g.8135_8148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.826_839del
ENST00000673647.1:c.-188-527_-188-514del	ENSP00000500967.1:n.-188-527_-188-514del
ENST00000673996.1:n.79+2135_79+2148del
ENST00000674069.1:c.-173+2155_-173+2168del	ENSP00000501157.1:n.-173+2155_-173+2168del
ENST00000674131.1:c.-188-527_-188-514del	ENSP00000501002.1:n.-188-527_-188-514del
ENST00000616296.4:c.-222+2135_-222+2148del	ENSP00000482382.1:n.-222+2135_-222+2148del
NM_001289152.1:c.-222+2135_-222+2148del	NP_001276081.1:n.-222+2135_-222+2148del
NM_001289153.1:c.-222+2155_-222+2168del	NP_001276082.1:n.-222+2155_-222+2168del
NM_001289154.1:c.-173+2155_-173+2168del	NP_001276083.1:n.-173+2155_-173+2168del
NM_001289152.2:c.-222+2135_-222+2148del	NP_001276081.1:n.-222+2135_-222+2148del
NM_001289153.2:c.-222+2155_-222+2168del	NP_001276082.1:n.-222+2155_-222+2168del
NM_001289154.2:c.-173+2155_-173+2168del	NP_001276083.1:n.-173+2155_-173+2168del