Canonical Allele Identifier: CA393175867

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188544T>G (hg19) ; chr15:g.74896203T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896203T>G , CM000677.2:g.74896203T>G	GRCh38
NC_000015.9:g.75188544T>G , CM000677.1:g.75188544T>G	GRCh37
NC_000015.8:g.72975597T>G	NCBI36
NG_008921.1:g.11135T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.722T>G MANE Select	ENSP00000318318.6:p.Leu241Arg
ENST00000323744.10:c.539T>G	ENSP00000318192.6:p.Leu180Arg
ENST00000352410.8:c.722T>G	ENSP00000318318.6:p.Leu241Arg
ENST00000535694.5:c.572T>G	ENSP00000440447.1:p.Leu191Arg
ENST00000562606.5:c.662T>G	ENSP00000457020.1:p.Leu221Arg
ENST00000562800.5:c.256-1336T>G	ENSP00000457619.1:n.256-1336T>G
ENST00000563422.5:c.722T>G	ENSP00000457885.1:p.Leu241Arg
ENST00000563786.5:c.662T>G	ENSP00000455241.1:p.Leu221Arg
ENST00000564003.5:c.389T>G	ENSP00000454312.1:p.Leu130Arg
ENST00000566377.5:c.722T>G	ENSP00000455405.1:p.Leu241Arg
ENST00000566556.1:n.770T>G
ENST00000567177.1:c.500T>G	ENSP00000457013.1:p.Leu167Arg
ENST00000569931.5:c.662T>G	ENSP00000455161.1:p.Leu221Arg
NM_001289155.1:c.722T>G	NP_001276084.1:p.Leu241Arg
NM_001289156.1:c.572T>G	NP_001276085.1:p.Leu191Arg
NM_001289157.1:c.539T>G	NP_001276086.1:p.Leu180Arg
NM_002435.2:c.722T>G	NP_002426.1:p.Leu241Arg
XM_011521592.1:c.710T>G	XP_011519894.1:p.Leu237Arg
XM_011521593.1:c.662T>G	XP_011519895.1:p.Leu221Arg
NM_001330372.1:c.662T>G	NP_001317301.1:p.Leu221Arg
XM_017022208.1:c.662T>G	XP_016877697.1:p.Leu221Arg
XM_017022209.2:c.572T>G	XP_016877698.1:p.Leu191Arg
NM_002435.3:c.722T>G MANE Select	NP_002426.1:p.Leu241Arg
NM_001289155.2:c.722T>G	NP_001276084.1:p.Leu241Arg
NM_001289156.2:c.572T>G	NP_001276085.1:p.Leu191Arg
NM_001289157.2:c.539T>G	NP_001276086.1:p.Leu180Arg
NM_001330372.2:c.662T>G	NP_001317301.1:p.Leu221Arg