Canonical Allele Identifier: CA449643540

Gene: MICA

Linked Data

• MyVariant Identifiers: chr6:g.31369969C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402192C>G , CM000668.2:g.31402192C>G	GRCh38
NC_000006.11:g.31369969C>G , CM000668.1:g.31369969C>G	GRCh37
NC_000006.10:g.31477948C>G	NCBI36
NG_034139.1:g.7409C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.100C>G
ENST00000673647.1:c.-353C>G	ENSP00000500967.1:n.-353C>G
ENST00000673996.1:n.79+1409C>G
ENST00000674069.1:c.-173+1429C>G	ENSP00000501157.1:n.-173+1429C>G
ENST00000674131.1:c.-353C>G	ENSP00000501002.1:n.-353C>G
ENST00000616296.4:c.-222+1409C>G	ENSP00000482382.1:n.-222+1409C>G
NM_001289152.1:c.-222+1409C>G	NP_001276081.1:n.-222+1409C>G
NM_001289153.1:c.-222+1429C>G	NP_001276082.1:n.-222+1429C>G
NM_001289154.1:c.-173+1429C>G	NP_001276083.1:n.-173+1429C>G
NM_001289152.2:c.-222+1409C>G	NP_001276081.1:n.-222+1409C>G
NM_001289153.2:c.-222+1429C>G	NP_001276082.1:n.-222+1429C>G
NM_001289154.2:c.-173+1429C>G	NP_001276083.1:n.-173+1429C>G