Allele Registry

Canonical Allele Identifier: CA14218033

Gene: MVP HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr16:g.29829904A>G

GRCh37 chr16:g.29841225A>G

Linked Data - Sequence & Population

gnomAD v2:

16:29841225 A / G

gnomAD v3:

16:29829904 A / G

gnomAD v4:

chr16-29829904-A-G

Joint Max Group AF 0.91379153 (AFR)

Genomes Max Group AF 0.91379153 (AFR)

Exomes Max Group AF 0.50731065 (NFE)

Linked Data - NCBI & NCI

dbSNP:

4788186

Genomic Alleles

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

Transcript Alleles

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

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