Canonical Allele Identifier: CA470851367

Gene: MINPP1

Linked Data

• MyVariant Identifiers: chr10:g.89268166T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508409T>A , CM000672.2:g.87508409T>A	GRCh38
NC_000010.10:g.89268166T>A , CM000672.1:g.89268166T>A	GRCh37
NC_000010.9:g.89258146T>A	NCBI36
NG_013023.1:g.8944T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371996.9:c.711T>A MANE Select	ENSP00000361064.4:p.Thr237=
ENST00000371994.8:c.711T>A	ENSP00000361062.4:p.Thr237=
ENST00000371996.8:c.711T>A	ENSP00000361064.4:p.Thr237=
ENST00000536010.1:c.108T>A	ENSP00000437823.1:p.Thr36=
NM_001178117.1:c.711T>A	NP_001171588.1:p.Thr237=
NM_001178118.1:c.108T>A	NP_001171589.1:p.Thr36=
NM_004897.4:c.711T>A	NP_004888.2:p.Thr237=
XM_006718078.2:c.711T>A	XP_006718141.1:p.Thr237=
XM_011540379.1:c.108T>A	XP_011538681.1:p.Thr36=
XR_945884.1:n.2835T>A
XM_006718078.3:c.711T>A	XP_006718141.1:p.Thr237=
XM_011540379.3:c.108T>A	XP_011538681.1:p.Thr36=
XM_017016965.2:c.711T>A	XP_016872454.1:p.Thr237=
NM_004897.5:c.711T>A MANE Select	NP_004888.2:p.Thr237=
NM_001178117.2:c.711T>A	NP_001171588.1:p.Thr237=
NM_001178118.2:c.108T>A	NP_001171589.1:p.Thr36=