Canonical Allele Identifier: CA393175771

Gene: MPI

Linked Data

• ClinVar Variation Id: 2676657
• ClinVar RCV Id: RCV003470171
• gnomAD v4: 15-74896160-G-T
• MyVariant Identifiers: chr15:g.75188501G>T (hg19) ; chr15:g.74896160G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896160G>T , CM000677.2:g.74896160G>T	GRCh38
NC_000015.9:g.75188501G>T , CM000677.1:g.75188501G>T	GRCh37
NC_000015.8:g.72975554G>T	NCBI36
NG_008921.1:g.11092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.679G>T MANE Select	ENSP00000318318.6:p.Gly227Ter
ENST00000323744.10:c.496G>T	ENSP00000318192.6:p.Gly166Ter
ENST00000352410.8:c.679G>T	ENSP00000318318.6:p.Gly227Ter
ENST00000535694.5:c.529G>T	ENSP00000440447.1:p.Gly177Ter
ENST00000561470.5:c.*575G>T	ENSP00000454267.1:n.*575G>T
ENST00000562606.5:c.619G>T	ENSP00000457020.1:p.Gly207Ter
ENST00000562800.5:c.256-1379G>T	ENSP00000457619.1:n.256-1379G>T
ENST00000563422.5:c.679G>T	ENSP00000457885.1:p.Gly227Ter
ENST00000563786.5:c.619G>T	ENSP00000455241.1:p.Gly207Ter
ENST00000564003.5:c.346G>T	ENSP00000454312.1:p.Gly116Ter
ENST00000566377.5:c.679G>T	ENSP00000455405.1:p.Gly227Ter
ENST00000566556.1:n.727G>T
ENST00000567177.1:c.457G>T	ENSP00000457013.1:p.Gly153Ter
ENST00000569931.5:c.619G>T	ENSP00000455161.1:p.Gly207Ter
NM_001289155.1:c.679G>T	NP_001276084.1:p.Gly227Ter
NM_001289156.1:c.529G>T	NP_001276085.1:p.Gly177Ter
NM_001289157.1:c.496G>T	NP_001276086.1:p.Gly166Ter
NM_002435.2:c.679G>T	NP_002426.1:p.Gly227Ter
XM_011521592.1:c.667G>T	XP_011519894.1:p.Gly223Ter
XM_011521593.1:c.619G>T	XP_011519895.1:p.Gly207Ter
NM_001330372.1:c.619G>T	NP_001317301.1:p.Gly207Ter
XM_017022208.1:c.619G>T	XP_016877697.1:p.Gly207Ter
XM_017022209.2:c.529G>T	XP_016877698.1:p.Gly177Ter
NM_002435.3:c.679G>T MANE Select	NP_002426.1:p.Gly227Ter
NM_001289155.2:c.679G>T	NP_001276084.1:p.Gly227Ter
NM_001289156.2:c.529G>T	NP_001276085.1:p.Gly177Ter
NM_001289157.2:c.496G>T	NP_001276086.1:p.Gly166Ter
NM_001330372.2:c.619G>T	NP_001317301.1:p.Gly207Ter