Canonical Allele Identifier: CA393169524

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75182968G>C (hg19) ; chr15:g.74890627G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890627G>C , CM000677.2:g.74890627G>C	GRCh38
NC_000015.9:g.75182968G>C , CM000677.1:g.75182968G>C	GRCh37
NC_000015.8:g.72970021G>C	NCBI36
NG_008921.1:g.5559G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.117G>C MANE Select	ENSP00000318318.6:p.Gln39His
ENST00000323744.10:c.117G>C	ENSP00000318192.6:p.Gln39His
ENST00000352410.8:c.117G>C	ENSP00000318318.6:p.Gln39His
ENST00000535694.5:c.-7+538G>C	ENSP00000440447.1:n.-7+538G>C
ENST00000561470.5:c.*13G>C	ENSP00000454267.1:n.*13G>C
ENST00000562606.5:c.57G>C	ENSP00000457020.1:p.Gln19His
ENST00000562800.5:c.117G>C	ENSP00000457619.1:p.Gln39His
ENST00000563422.5:c.117G>C	ENSP00000457885.1:p.Gln39His
ENST00000563786.5:c.57G>C	ENSP00000455241.1:p.Gln19His
ENST00000564003.5:c.-7+538G>C	ENSP00000454312.1:n.-7+538G>C
ENST00000564633.5:c.57G>C	ENSP00000455383.1:p.Gln19His
ENST00000565576.5:c.117G>C	ENSP00000454619.1:p.Gln39His
ENST00000566377.5:c.117G>C	ENSP00000455405.1:p.Gln39His
ENST00000567116.5:n.148G>C
ENST00000567132.5:c.117G>C	ENSP00000455972.1:p.Gln39His
ENST00000567177.1:c.78G>C	ENSP00000457013.1:p.Gln26His
ENST00000567570.5:c.57G>C	ENSP00000455477.1:p.Gln19His
ENST00000568303.1:n.234G>C
ENST00000568828.5:c.117G>C	ENSP00000455065.1:p.Gln39His
ENST00000568840.1:n.226G>C
ENST00000568907.5:c.117G>C	ENSP00000457494.1:p.Gln39His
ENST00000569233.5:c.117G>C	ENSP00000454622.1:p.Gln39His
ENST00000569931.5:c.57G>C	ENSP00000455161.1:p.Gln19His
NM_001289155.1:c.117G>C	NP_001276084.1:p.Gln39His
NM_001289156.1:c.-7+538G>C	NP_001276085.1:n.-7+538G>C
NM_001289157.1:c.117G>C	NP_001276086.1:p.Gln39His
NM_002435.2:c.117G>C	NP_002426.1:p.Gln39His
XM_011521592.1:c.105G>C	XP_011519894.1:p.Gln35His
XM_011521593.1:c.57G>C	XP_011519895.1:p.Gln19His
NM_001330372.1:c.57G>C	NP_001317301.1:p.Gln19His
XM_017022208.1:c.57G>C	XP_016877697.1:p.Gln19His
XM_017022209.2:c.-7+538G>C	XP_016877698.1:n.-7+538G>C
NM_002435.3:c.117G>C MANE Select	NP_002426.1:p.Gln39His
NM_001289155.2:c.117G>C	NP_001276084.1:p.Gln39His
NM_001289156.2:c.-7+538G>C	NP_001276085.1:n.-7+538G>C
NM_001289157.2:c.117G>C	NP_001276086.1:p.Gln39His
NM_001330372.2:c.57G>C	NP_001317301.1:p.Gln19His