Canonical Allele Identifier: CA338460778

Gene: MIIP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12022869A>T , CM000663.2:g.12022869A>T	GRCh38
NC_000001.10:g.12082926A>T , CM000663.1:g.12082926A>T	GRCh37
NC_000001.9:g.12005513A>T	NCBI36
NG_030022.1:g.8628A>T
NG_030022.2:g.8628A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021933.4:c.499A>T MANE Select	NP_068752.2:p.Lys167Ter
ENST00000235332.6:c.499A>T MANE Select	ENSP00000235332.4:p.Lys167Ter
NM_021933.3:c.499A>T	NP_068752.2:p.Lys167Ter
ENST00000235332.5:c.499A>T	ENSP00000235332.4:p.Lys167Ter
ENST00000466860.5:n.258A>T
ENST00000478749.5:n.472A>T
ENST00000498685.5:n.6A>T
XM_005263487.2:c.499A>T	XP_005263544.1:p.Lys167Ter
XM_005263487.4:c.499A>T	XP_005263544.1:p.Lys167Ter
XM_011541895.1:c.499A>T	XP_011540197.1:p.Lys167Ter
XM_011541896.1:c.499A>T	XP_011540198.1:p.Lys167Ter