Canonical Allele Identifier: CA5589073

Gene: MINPP1

Linked Data

• dbSNP Id: rs748152849
• ExAC: 10:89268076 A / T
• gnomAD v2: 10-89268076-A-T
• gnomAD v3: 10-87508319-A-T
• gnomAD v4: 10-87508319-A-T
• MyVariant Identifiers: chr10:g.89268076A>T (hg19) ; chr10:g.87508319A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508319A>T , CM000672.2:g.87508319A>T	GRCh38
NC_000010.10:g.89268076A>T , CM000672.1:g.89268076A>T	GRCh37
NC_000010.9:g.89258056A>T	NCBI36
NG_013023.1:g.8854A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371996.9:c.638-17A>T MANE Select	ENSP00000361064.4:n.638-17A>T
ENST00000371994.8:c.638-17A>T	ENSP00000361062.4:n.638-17A>T
ENST00000371996.8:c.638-17A>T	ENSP00000361064.4:n.638-17A>T
ENST00000536010.1:c.35-17A>T	ENSP00000437823.1:n.35-17A>T
NM_001178117.1:c.638-17A>T	NP_001171588.1:n.638-17A>T
NM_001178118.1:c.35-17A>T	NP_001171589.1:n.35-17A>T
NM_004897.4:c.638-17A>T	NP_004888.2:n.638-17A>T
XM_006718078.2:c.638-17A>T	XP_006718141.1:n.638-17A>T
XM_011540379.1:c.35-17A>T	XP_011538681.1:n.35-17A>T
XR_945884.1:n.2762-17A>T
XM_006718078.3:c.638-17A>T	XP_006718141.1:n.638-17A>T
XM_011540379.3:c.35-17A>T	XP_011538681.1:n.35-17A>T
XM_017016965.2:c.638-17A>T	XP_016872454.1:n.638-17A>T
NM_004897.5:c.638-17A>T MANE Select	NP_004888.2:n.638-17A>T
NM_001178117.2:c.638-17A>T	NP_001171588.1:n.638-17A>T
NM_001178118.2:c.35-17A>T	NP_001171589.1:n.35-17A>T