Canonical Allele Identifier: CA470851388

Gene: MINPP1

Linked Data

• gnomAD v4: 10-87508415-A-G
• MyVariant Identifiers: chr10:g.89268172A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508415A>G , CM000672.2:g.87508415A>G	GRCh38
NC_000010.10:g.89268172A>G , CM000672.1:g.89268172A>G	GRCh37
NC_000010.9:g.89258152A>G	NCBI36
NG_013023.1:g.8950A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.717A>G MANE Select	ENSP00000361064.4:p.Val239=
ENST00000371994.8:c.717A>G	ENSP00000361062.4:p.Val239=
ENST00000371996.8:c.717A>G	ENSP00000361064.4:p.Val239=
ENST00000536010.1:c.114A>G	ENSP00000437823.1:p.Val38=
NM_001178117.1:c.717A>G	NP_001171588.1:p.Val239=
NM_001178118.1:c.114A>G	NP_001171589.1:p.Val38=
NM_004897.4:c.717A>G	NP_004888.2:p.Val239=
XM_006718078.2:c.717A>G	XP_006718141.1:p.Val239=
XM_011540379.1:c.114A>G	XP_011538681.1:p.Val38=
XR_945884.1:n.2841A>G
XM_006718078.3:c.717A>G	XP_006718141.1:p.Val239=
XM_011540379.3:c.114A>G	XP_011538681.1:p.Val38=
XM_017016965.2:c.717A>G	XP_016872454.1:p.Val239=
NM_004897.5:c.717A>G MANE Select	NP_004888.2:p.Val239=
NM_001178117.2:c.717A>G	NP_001171588.1:p.Val239=
NM_001178118.2:c.114A>G	NP_001171589.1:p.Val38=