Canonical Allele Identifier: CA393175969

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188591C>A (hg19) ; chr15:g.74896250C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896250C>A , CM000677.2:g.74896250C>A	GRCh38
NC_000015.9:g.75188591C>A , CM000677.1:g.75188591C>A	GRCh37
NC_000015.8:g.72975644C>A	NCBI36
NG_008921.1:g.11182C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.769C>A MANE Select	ENSP00000318318.6:p.Leu257Met
ENST00000323744.10:c.586C>A	ENSP00000318192.6:p.Leu196Met
ENST00000352410.8:c.769C>A	ENSP00000318318.6:p.Leu257Met
ENST00000535694.5:c.619C>A	ENSP00000440447.1:p.Leu207Met
ENST00000562606.5:c.709C>A	ENSP00000457020.1:p.Leu237Met
ENST00000562800.5:c.256-1289C>A	ENSP00000457619.1:n.256-1289C>A
ENST00000563422.5:c.769C>A	ENSP00000457885.1:p.Leu257Met
ENST00000563786.5:c.709C>A	ENSP00000455241.1:p.Leu237Met
ENST00000564003.5:c.436C>A	ENSP00000454312.1:p.Leu146Met
ENST00000566377.5:c.769C>A	ENSP00000455405.1:p.Leu257Met
ENST00000566556.1:n.817C>A
ENST00000567177.1:c.547C>A	ENSP00000457013.1:p.Leu183Met
ENST00000569931.5:c.709C>A	ENSP00000455161.1:p.Leu237Met
NM_001289155.1:c.769C>A	NP_001276084.1:p.Leu257Met
NM_001289156.1:c.619C>A	NP_001276085.1:p.Leu207Met
NM_001289157.1:c.586C>A	NP_001276086.1:p.Leu196Met
NM_002435.2:c.769C>A	NP_002426.1:p.Leu257Met
XM_011521592.1:c.757C>A	XP_011519894.1:p.Leu253Met
XM_011521593.1:c.709C>A	XP_011519895.1:p.Leu237Met
NM_001330372.1:c.709C>A	NP_001317301.1:p.Leu237Met
XM_017022208.1:c.709C>A	XP_016877697.1:p.Leu237Met
XM_017022209.2:c.619C>A	XP_016877698.1:p.Leu207Met
NM_002435.3:c.769C>A MANE Select	NP_002426.1:p.Leu257Met
NM_001289155.2:c.769C>A	NP_001276084.1:p.Leu257Met
NM_001289156.2:c.619C>A	NP_001276085.1:p.Leu207Met
NM_001289157.2:c.586C>A	NP_001276086.1:p.Leu196Met
NM_001330372.2:c.709C>A	NP_001317301.1:p.Leu237Met