Canonical Allele Identifier: CA2677963034

Gene: MICA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31403810C>T , CM000668.2:g.31403810C>T	GRCh38
NC_000006.11:g.31371587C>T , CM000668.1:g.31371587C>T	GRCh37
NC_000006.10:g.31479566C>T	NCBI36
NG_034139.1:g.9027C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001177519.3:c.70+108C>T MANE Select	NP_001170990.1:n.70+108C>T
ENST00000449934.7:c.70+108C>T MANE Select	ENSP00000413079.1:n.70+108C>T
NM_001177519.2:c.70+108C>T	NP_001170990.1:n.70+108C>T
NM_001289152.1:c.-222+3027C>T	NP_001276081.1:n.-222+3027C>T
NM_001289152.2:c.-222+3027C>T	NP_001276081.1:n.-222+3027C>T
NM_001289153.1:c.-222+3047C>T	NP_001276082.1:n.-222+3047C>T
NM_001289153.2:c.-222+3047C>T	NP_001276082.1:n.-222+3047C>T
NM_001289154.1:c.-173+3047C>T	NP_001276083.1:n.-173+3047C>T
NM_001289154.2:c.-173+3047C>T	NP_001276083.1:n.-173+3047C>T
ENST00000421350.1:c.31+108C>T	ENSP00000402410.1:n.31+108C>T
ENST00000449934.6:c.70+108C>T	ENSP00000413079.1:n.70+108C>T
ENST00000616296.4:c.-222+3027C>T	ENSP00000482382.1:n.-222+3027C>T
ENST00000673647.1:c.70+108C>T	ENSP00000500967.1:n.70+108C>T
ENST00000673996.1:n.79+3027C>T
ENST00000674069.1:c.-173+3047C>T	ENSP00000501157.1:n.-173+3047C>T