Canonical Allele Identifier: CA2187902041

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896356_74896357delinsGC , CM000677.2:g.74896356_74896357delinsGC	GRCh38
NC_000015.9:g.75188697_75188698delinsGC , CM000677.1:g.75188697_75188698delinsGC	GRCh37
NC_000015.8:g.72975750_72975751delinsGC	NCBI36
NG_008921.1:g.11288_11289delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+31_844+32delinsGC MANE Select	ENSP00000318318.6:n.844+31_844+32delinsGC
ENST00000323744.10:c.661+31_661+32delinsGC	ENSP00000318192.6:n.661+31_661+32delinsGC
ENST00000352410.8:c.844+31_844+32delinsGC	ENSP00000318318.6:n.844+31_844+32delinsGC
ENST00000535694.5:c.694+31_694+32delinsGC	ENSP00000440447.1:n.694+31_694+32delinsGC
ENST00000562606.5:c.815_816delinsGC	ENSP00000457020.1:p.Cys272=
ENST00000562800.5:c.256-1183_256-1182delinsGC	ENSP00000457619.1:n.256-1183_256-1182delinsGC
ENST00000563422.5:c.875_876delinsGC	ENSP00000457885.1:p.Cys292=
ENST00000563786.5:c.784+31_784+32delinsGC	ENSP00000455241.1:n.784+31_784+32delinsGC
ENST00000564003.5:c.542_543delinsGC	ENSP00000454312.1:p.Cys181=
ENST00000566377.5:c.844+31_844+32delinsGC	ENSP00000455405.1:n.844+31_844+32delinsGC
ENST00000566556.1:n.923_924delinsGC
ENST00000567177.1:c.622+31_622+32delinsGC	ENSP00000457013.1:n.622+31_622+32delinsGC
ENST00000569931.5:c.784+31_784+32delinsGC	ENSP00000455161.1:n.784+31_784+32delinsGC
NM_001289155.1:c.844+31_844+32delinsGC	NP_001276084.1:n.844+31_844+32delinsGC
NM_001289156.1:c.694+31_694+32delinsGC	NP_001276085.1:n.694+31_694+32delinsGC
NM_001289157.1:c.661+31_661+32delinsGC	NP_001276086.1:n.661+31_661+32delinsGC
NM_002435.2:c.844+31_844+32delinsGC	NP_002426.1:n.844+31_844+32delinsGC
XM_011521592.1:c.832+31_832+32delinsGC	XP_011519894.1:n.832+31_832+32delinsGC
XM_011521593.1:c.784+31_784+32delinsGC	XP_011519895.1:n.784+31_784+32delinsGC
NM_001330372.1:c.784+31_784+32delinsGC	NP_001317301.1:n.784+31_784+32delinsGC
XM_017022208.1:c.784+31_784+32delinsGC	XP_016877697.1:n.784+31_784+32delinsGC
XM_017022209.2:c.694+31_694+32delinsGC	XP_016877698.1:n.694+31_694+32delinsGC
NM_002435.3:c.844+31_844+32delinsGC MANE Select	NP_002426.1:n.844+31_844+32delinsGC
NM_001289155.2:c.844+31_844+32delinsGC	NP_001276084.1:n.844+31_844+32delinsGC
NM_001289156.2:c.694+31_694+32delinsGC	NP_001276085.1:n.694+31_694+32delinsGC
NM_001289157.2:c.661+31_661+32delinsGC	NP_001276086.1:n.661+31_661+32delinsGC
NM_001330372.2:c.784+31_784+32delinsGC	NP_001317301.1:n.784+31_784+32delinsGC