Canonical Allele Identifier: CA7662537

Gene: MPI

Linked Data

• dbSNP Id: rs191159836
• ExAC: 15:75188575 C / G
• gnomAD v2: 15-75188575-C-G
• gnomAD v4: 15-74896234-C-G
• MyVariant Identifiers: chr15:g.75188575C>G (hg19) ; chr15:g.74896234C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896234C>G , CM000677.2:g.74896234C>G	GRCh38
NC_000015.9:g.75188575C>G , CM000677.1:g.75188575C>G	GRCh37
NC_000015.8:g.72975628C>G	NCBI36
NG_008921.1:g.11166C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.753C>G MANE Select	ENSP00000318318.6:p.Cys251Trp
ENST00000323744.10:c.570C>G	ENSP00000318192.6:p.Cys190Trp
ENST00000352410.8:c.753C>G	ENSP00000318318.6:p.Cys251Trp
ENST00000535694.5:c.603C>G	ENSP00000440447.1:p.Cys201Trp
ENST00000562606.5:c.693C>G	ENSP00000457020.1:p.Cys231Trp
ENST00000562800.5:c.256-1305C>G	ENSP00000457619.1:n.256-1305C>G
ENST00000563422.5:c.753C>G	ENSP00000457885.1:p.Cys251Trp
ENST00000563786.5:c.693C>G	ENSP00000455241.1:p.Cys231Trp
ENST00000564003.5:c.420C>G	ENSP00000454312.1:p.Cys140Trp
ENST00000566377.5:c.753C>G	ENSP00000455405.1:p.Cys251Trp
ENST00000566556.1:n.801C>G
ENST00000567177.1:c.531C>G	ENSP00000457013.1:p.Cys177Trp
ENST00000569931.5:c.693C>G	ENSP00000455161.1:p.Cys231Trp
NM_001289155.1:c.753C>G	NP_001276084.1:p.Cys251Trp
NM_001289156.1:c.603C>G	NP_001276085.1:p.Cys201Trp
NM_001289157.1:c.570C>G	NP_001276086.1:p.Cys190Trp
NM_002435.2:c.753C>G	NP_002426.1:p.Cys251Trp
XM_011521592.1:c.741C>G	XP_011519894.1:p.Cys247Trp
XM_011521593.1:c.693C>G	XP_011519895.1:p.Cys231Trp
NM_001330372.1:c.693C>G	NP_001317301.1:p.Cys231Trp
XM_017022208.1:c.693C>G	XP_016877697.1:p.Cys231Trp
XM_017022209.2:c.603C>G	XP_016877698.1:p.Cys201Trp
NM_002435.3:c.753C>G MANE Select	NP_002426.1:p.Cys251Trp
NM_001289155.2:c.753C>G	NP_001276084.1:p.Cys251Trp
NM_001289156.2:c.603C>G	NP_001276085.1:p.Cys201Trp
NM_001289157.2:c.570C>G	NP_001276086.1:p.Cys190Trp
NM_001330372.2:c.693C>G	NP_001317301.1:p.Cys231Trp