Canonical Allele Identifier: CA2677962447

Gene: MICA

Linked Data

• gnomAD v4: 6-31402251-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402253_31402254del , CM000668.2:g.31402253_31402254del	GRCh38
NC_000006.11:g.31370030_31370031del , CM000668.1:g.31370030_31370031del	GRCh37
NC_000006.10:g.31478009_31478010del	NCBI36
NG_034139.1:g.7470_7471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.161_162del
ENST00000673647.1:c.-292_-291del	ENSP00000500967.1:n.-292_-291del
ENST00000673996.1:n.79+1470_79+1471del
ENST00000674069.1:c.-173+1490_-173+1491del	ENSP00000501157.1:n.-173+1490_-173+1491del
ENST00000674131.1:c.-292_-291del	ENSP00000501002.1:n.-292_-291del
ENST00000616296.4:c.-222+1470_-222+1471del	ENSP00000482382.1:n.-222+1470_-222+1471del
NM_001289152.1:c.-222+1470_-222+1471del	NP_001276081.1:n.-222+1470_-222+1471del
NM_001289153.1:c.-222+1490_-222+1491del	NP_001276082.1:n.-222+1490_-222+1491del
NM_001289154.1:c.-173+1490_-173+1491del	NP_001276083.1:n.-173+1490_-173+1491del
NM_001289152.2:c.-222+1470_-222+1471del	NP_001276081.1:n.-222+1470_-222+1471del
NM_001289153.2:c.-222+1490_-222+1491del	NP_001276082.1:n.-222+1490_-222+1491del
NM_001289154.2:c.-173+1490_-173+1491del	NP_001276083.1:n.-173+1490_-173+1491del