Canonical Allele Identifier: CA377782571

Gene: MINPP1

Linked Data

• gnomAD v4: 10-87508414-T-C
• MyVariant Identifiers: chr10:g.89268171T>C (hg19) ; chr10:g.87508414T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508414T>C , CM000672.2:g.87508414T>C	GRCh38
NC_000010.10:g.89268171T>C , CM000672.1:g.89268171T>C	GRCh37
NC_000010.9:g.89258151T>C	NCBI36
NG_013023.1:g.8949T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.716T>C MANE Select	ENSP00000361064.4:p.Val239Ala
ENST00000371994.8:c.716T>C	ENSP00000361062.4:p.Val239Ala
ENST00000371996.8:c.716T>C	ENSP00000361064.4:p.Val239Ala
ENST00000536010.1:c.113T>C	ENSP00000437823.1:p.Val38Ala
NM_001178117.1:c.716T>C	NP_001171588.1:p.Val239Ala
NM_001178118.1:c.113T>C	NP_001171589.1:p.Val38Ala
NM_004897.4:c.716T>C	NP_004888.2:p.Val239Ala
XM_006718078.2:c.716T>C	XP_006718141.1:p.Val239Ala
XM_011540379.1:c.113T>C	XP_011538681.1:p.Val38Ala
XR_945884.1:n.2840T>C
XM_006718078.3:c.716T>C	XP_006718141.1:p.Val239Ala
XM_011540379.3:c.113T>C	XP_011538681.1:p.Val38Ala
XM_017016965.2:c.716T>C	XP_016872454.1:p.Val239Ala
NM_004897.5:c.716T>C MANE Select	NP_004888.2:p.Val239Ala
NM_001178117.2:c.716T>C	NP_001171588.1:p.Val239Ala
NM_001178118.2:c.113T>C	NP_001171589.1:p.Val38Ala