Canonical Allele Identifier: CA2216321289

Gene: MVP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29829904A= , CM000678.2:g.29829904A=	GRCh38
NC_000016.9:g.29841225A= , CM000678.1:g.29841225A=	GRCh37
NC_000016.8:g.29748726A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005115.5:c.-35-611A= MANE Select	NP_005106.2:n.-35-611A=
ENST00000357402.10:c.-35-611A= MANE Select	ENSP00000349977.5:n.-35-611A=
NM_005115.4:c.-35-611A=	NP_005106.2:n.-35-611A=
NM_017458.3:c.-76-570A=	NP_059447.2:n.-76-570A=
ENST00000357402.9:c.-35-611A=	ENSP00000349977.5:n.-35-611A=
ENST00000395353.5:c.-76-570A=	ENSP00000378760.1:n.-76-570A=
ENST00000562285.1:c.403-570A=
ENST00000562463.5:c.-35-611A=	ENSP00000457734.1:n.-35-611A=
ENST00000563096.1:n.46-570A=
ENST00000563558.5:c.-76-570A=	ENSP00000454825.1:n.-76-570A=
ENST00000563915.5:c.-76-570A=	ENSP00000455819.1:n.-76-570A=
ENST00000565164.1:c.-35-611A=	ENSP00000454819.1:n.-35-611A=
ENST00000565830.5:n.35-570A=
ENST00000566066.5:c.-76-570A=	ENSP00000455186.1:n.-76-570A=
ENST00000566252.1:c.-36+242A=	ENSP00000457685.1:n.-36+242A=
ENST00000566554.1:n.175A=
ENST00000566859.5:c.-35-611A=	ENSP00000455741.1:n.-35-611A=
ENST00000569887.1:c.-35-611A=	ENSP00000455532.1:n.-35-611A=
ENST00000570234.5:c.-35-611A=	ENSP00000456291.1:n.-35-611A=