Canonical Allele Identifier: CA912992716

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188623_75188625del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896282_74896284del , CM000677.2:g.74896282_74896284del	GRCh38
NC_000015.9:g.75188623_75188625del , CM000677.1:g.75188623_75188625del	GRCh37
NC_000015.8:g.72975676_72975678del	NCBI36
NG_008921.1:g.11214_11216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.801_803del MANE Select	ENSP00000318318.6:p.Met268del
ENST00000323744.10:c.618_620del	ENSP00000318192.6:p.Met207del
ENST00000352410.8:c.801_803del	ENSP00000318318.6:p.Met268del
ENST00000535694.5:c.651_653del	ENSP00000440447.1:p.Met218del
ENST00000562606.5:c.741_743del	ENSP00000457020.1:p.Met248del
ENST00000562800.5:c.256-1257_256-1255del	ENSP00000457619.1:n.256-1257_256-1255del
ENST00000563422.5:c.801_803del	ENSP00000457885.1:p.Met268del
ENST00000563786.5:c.741_743del	ENSP00000455241.1:p.Met248del
ENST00000564003.5:c.468_470del	ENSP00000454312.1:p.Met157del
ENST00000566377.5:c.801_803del	ENSP00000455405.1:p.Met268del
ENST00000566556.1:n.849_851del
ENST00000567177.1:c.579_581del	ENSP00000457013.1:p.Met194del
ENST00000569931.5:c.741_743del	ENSP00000455161.1:p.Met248del
NM_001289155.1:c.801_803del	NP_001276084.1:p.Met268del
NM_001289156.1:c.651_653del	NP_001276085.1:p.Met218del
NM_001289157.1:c.618_620del	NP_001276086.1:p.Met207del
NM_002435.2:c.801_803del	NP_002426.1:p.Met268del
XM_011521592.1:c.789_791del	XP_011519894.1:p.Met264del
XM_011521593.1:c.741_743del	XP_011519895.1:p.Met248del
NM_001330372.1:c.741_743del	NP_001317301.1:p.Met248del
XM_017022208.1:c.741_743del	XP_016877697.1:p.Met248del
XM_017022209.2:c.651_653del	XP_016877698.1:p.Met218del
NM_002435.3:c.801_803del MANE Select	NP_002426.1:p.Met268del
NM_001289155.2:c.801_803del	NP_001276084.1:p.Met268del
NM_001289156.2:c.651_653del	NP_001276085.1:p.Met218del
NM_001289157.2:c.618_620del	NP_001276086.1:p.Met207del
NM_001330372.2:c.741_743del	NP_001317301.1:p.Met248del