Canonical Allele Identifier: CA2629528532

Gene: MPI

Linked Data

• gnomAD v4: 15-74891278-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74891279_74891280del , CM000677.2:g.74891279_74891280del	GRCh38
NC_000015.9:g.75183620_75183621del , CM000677.1:g.75183620_75183621del	GRCh37
NC_000015.8:g.72970673_72970674del	NCBI36
NG_008921.1:g.6211_6212del

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.145-100_145-99del MANE Select	ENSP00000318318.6:n.145-100_145-99del
ENST00000323744.10:c.145-100_145-99del	ENSP00000318192.6:n.145-100_145-99del
ENST00000352410.8:c.145-100_145-99del	ENSP00000318318.6:n.145-100_145-99del
ENST00000535694.5:c.-6-100_-6-99del	ENSP00000440447.1:n.-6-100_-6-99del
ENST00000561470.5:c.*41-100_*41-99del	ENSP00000454267.1:n.*41-100_*41-99del
ENST00000562606.5:c.85-100_85-99del	ENSP00000457020.1:n.85-100_85-99del
ENST00000562800.5:c.145-100_145-99del	ENSP00000457619.1:n.145-100_145-99del
ENST00000563422.5:c.145-100_145-99del	ENSP00000457885.1:n.145-100_145-99del
ENST00000563786.5:c.85-100_85-99del	ENSP00000455241.1:n.85-100_85-99del
ENST00000564003.5:c.-6-100_-6-99del	ENSP00000454312.1:n.-6-100_-6-99del
ENST00000564633.5:c.85-100_85-99del	ENSP00000455383.1:n.85-100_85-99del
ENST00000565576.5:c.145-100_145-99del	ENSP00000454619.1:n.145-100_145-99del
ENST00000566377.5:c.145-100_145-99del	ENSP00000455405.1:n.145-100_145-99del
ENST00000567116.5:n.176-100_176-99del
ENST00000567132.5:c.145-100_145-99del	ENSP00000455972.1:n.145-100_145-99del
ENST00000567177.1:c.106-100_106-99del	ENSP00000457013.1:n.106-100_106-99del
ENST00000567570.5:c.85-100_85-99del	ENSP00000455477.1:n.85-100_85-99del
ENST00000568828.5:c.145-136_145-135del	ENSP00000455065.1:n.145-136_145-135del
ENST00000568840.1:n.254-100_254-99del
ENST00000568907.5:c.145-100_145-99del	ENSP00000457494.1:n.145-100_145-99del
ENST00000569233.5:c.202-100_202-99del	ENSP00000454622.1:n.202-100_202-99del
ENST00000569931.5:c.85-100_85-99del	ENSP00000455161.1:n.85-100_85-99del
NM_001289155.1:c.145-100_145-99del	NP_001276084.1:n.145-100_145-99del
NM_001289156.1:c.-6-100_-6-99del	NP_001276085.1:n.-6-100_-6-99del
NM_001289157.1:c.145-100_145-99del	NP_001276086.1:n.145-100_145-99del
NM_002435.2:c.145-100_145-99del	NP_002426.1:n.145-100_145-99del
XM_011521592.1:c.133-100_133-99del	XP_011519894.1:n.133-100_133-99del
XM_011521593.1:c.85-100_85-99del	XP_011519895.1:n.85-100_85-99del
NM_001330372.1:c.85-100_85-99del	NP_001317301.1:n.85-100_85-99del
XM_017022208.1:c.85-100_85-99del	XP_016877697.1:n.85-100_85-99del
XM_017022209.2:c.-6-100_-6-99del	XP_016877698.1:n.-6-100_-6-99del
NM_002435.3:c.145-100_145-99del MANE Select	NP_002426.1:n.145-100_145-99del
NM_001289155.2:c.145-100_145-99del	NP_001276084.1:n.145-100_145-99del
NM_001289156.2:c.-6-100_-6-99del	NP_001276085.1:n.-6-100_-6-99del
NM_001289157.2:c.145-100_145-99del	NP_001276086.1:n.145-100_145-99del
NM_001330372.2:c.85-100_85-99del	NP_001317301.1:n.85-100_85-99del