Canonical Allele Identifier: CA971516569

Gene: MPI

Linked Data

• dbSNP Id: rs2064705512
• gnomAD v3: 15-74890359-A-ATCT
• gnomAD v4: 15-74890359-A-ATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890359_74890360insTCT , CM000677.2:g.74890359_74890360insTCT	GRCh38
NC_000015.9:g.75182700_75182701insTCT , CM000677.1:g.75182700_75182701insTCT	GRCh37
NC_000015.8:g.72969753_72969754insTCT	NCBI36
NG_008921.1:g.5291_5292insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.17-168_17-167insTCT MANE Select	ENSP00000318318.6:n.17-168_17-167insTCT
ENST00000323744.10:c.17-168_17-167insTCT	ENSP00000318192.6:n.17-168_17-167insTCT
ENST00000352410.8:c.17-168_17-167insTCT	ENSP00000318318.6:n.17-168_17-167insTCT
ENST00000535694.5:c.-7+270_-7+271insTCT	ENSP00000440447.1:n.-7+270_-7+271insTCT
ENST00000561470.5:c.128+158_128+159insTCT	ENSP00000454267.1:n.128+158_128+159insTCT
ENST00000562606.5:c.-18-194_-18-193insTCT	ENSP00000457020.1:n.-18-194_-18-193insTCT
ENST00000562800.5:c.17-168_17-167insTCT	ENSP00000457619.1:n.17-168_17-167insTCT
ENST00000563422.5:c.17-168_17-167insTCT	ENSP00000457885.1:n.17-168_17-167insTCT
ENST00000563786.5:c.-133-79_-133-78insTCT	ENSP00000455241.1:n.-133-79_-133-78insTCT
ENST00000564003.5:c.-7+270_-7+271insTCT	ENSP00000454312.1:n.-7+270_-7+271insTCT
ENST00000564633.5:c.-15-197_-15-196insTCT	ENSP00000455383.1:n.-15-197_-15-196insTCT
ENST00000565576.5:c.17-168_17-167insTCT	ENSP00000454619.1:n.17-168_17-167insTCT
ENST00000566377.5:c.17-168_17-167insTCT	ENSP00000455405.1:n.17-168_17-167insTCT
ENST00000567116.5:n.48-168_48-167insTCT
ENST00000567132.5:c.17-168_17-167insTCT	ENSP00000455972.1:n.17-168_17-167insTCT
ENST00000567570.5:c.-212_-211insTCT	ENSP00000455477.1:n.-212_-211insTCT
ENST00000568303.1:n.45-79_45-78insTCT
ENST00000568828.5:c.17-168_17-167insTCT	ENSP00000455065.1:n.17-168_17-167insTCT
ENST00000568840.1:n.125+158_125+159insTCT
ENST00000568907.5:c.17-168_17-167insTCT	ENSP00000457494.1:n.17-168_17-167insTCT
ENST00000569233.5:c.17-168_17-167insTCT	ENSP00000454622.1:n.17-168_17-167insTCT
ENST00000569931.5:c.-18-194_-18-193insTCT	ENSP00000455161.1:n.-18-194_-18-193insTCT
NM_001289155.1:c.17-168_17-167insTCT	NP_001276084.1:n.17-168_17-167insTCT
NM_001289156.1:c.-7+270_-7+271insTCT	NP_001276085.1:n.-7+270_-7+271insTCT
NM_001289157.1:c.17-168_17-167insTCT	NP_001276086.1:n.17-168_17-167insTCT
NM_002435.2:c.17-168_17-167insTCT	NP_002426.1:n.17-168_17-167insTCT
XM_011521592.1:c.4+158_4+159insTCT	XP_011519894.1:n.4+158_4+159insTCT
XM_011521593.1:c.-133-79_-133-78insTCT	XP_011519895.1:n.-133-79_-133-78insTCT
NM_001330372.1:c.-133-79_-133-78insTCT	NP_001317301.1:n.-133-79_-133-78insTCT
XM_017022208.1:c.-133-79_-133-78insTCT	XP_016877697.1:n.-133-79_-133-78insTCT
XM_017022209.2:c.-7+270_-7+271insTCT	XP_016877698.1:n.-7+270_-7+271insTCT
NM_002435.3:c.17-168_17-167insTCT MANE Select	NP_002426.1:n.17-168_17-167insTCT
NM_001289155.2:c.17-168_17-167insTCT	NP_001276084.1:n.17-168_17-167insTCT
NM_001289156.2:c.-7+270_-7+271insTCT	NP_001276085.1:n.-7+270_-7+271insTCT
NM_001289157.2:c.17-168_17-167insTCT	NP_001276086.1:n.17-168_17-167insTCT
NM_001330372.2:c.-133-79_-133-78insTCT	NP_001317301.1:n.-133-79_-133-78insTCT