Canonical Allele Identifier: CA377782567

Gene: MINPP1

Linked Data

• MyVariant Identifiers: chr10:g.89268170G>A (hg19) ; chr10:g.87508413G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508413G>A , CM000672.2:g.87508413G>A	GRCh38
NC_000010.10:g.89268170G>A , CM000672.1:g.89268170G>A	GRCh37
NC_000010.9:g.89258150G>A	NCBI36
NG_013023.1:g.8948G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.715G>A MANE Select	ENSP00000361064.4:p.Val239Ile
ENST00000371994.8:c.715G>A	ENSP00000361062.4:p.Val239Ile
ENST00000371996.8:c.715G>A	ENSP00000361064.4:p.Val239Ile
ENST00000536010.1:c.112G>A	ENSP00000437823.1:p.Val38Ile
NM_001178117.1:c.715G>A	NP_001171588.1:p.Val239Ile
NM_001178118.1:c.112G>A	NP_001171589.1:p.Val38Ile
NM_004897.4:c.715G>A	NP_004888.2:p.Val239Ile
XM_006718078.2:c.715G>A	XP_006718141.1:p.Val239Ile
XM_011540379.1:c.112G>A	XP_011538681.1:p.Val38Ile
XR_945884.1:n.2839G>A
XM_006718078.3:c.715G>A	XP_006718141.1:p.Val239Ile
XM_011540379.3:c.112G>A	XP_011538681.1:p.Val38Ile
XM_017016965.2:c.715G>A	XP_016872454.1:p.Val239Ile
NM_004897.5:c.715G>A MANE Select	NP_004888.2:p.Val239Ile
NM_001178117.2:c.715G>A	NP_001171588.1:p.Val239Ile
NM_001178118.2:c.112G>A	NP_001171589.1:p.Val38Ile