Canonical Allele Identifier: CA393174487

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75185554A>C (hg19) ; chr15:g.74893213A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74893213A>C , CM000677.2:g.74893213A>C	GRCh38
NC_000015.9:g.75185554A>C , CM000677.1:g.75185554A>C	GRCh37
NC_000015.8:g.72972607A>C	NCBI36
NG_008921.1:g.8145A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.563A>C MANE Select	ENSP00000318318.6:p.Gln188Pro
ENST00000323744.10:c.487+411A>C	ENSP00000318192.6:n.487+411A>C
ENST00000352410.8:c.563A>C	ENSP00000318318.6:p.Gln188Pro
ENST00000535694.5:c.413A>C	ENSP00000440447.1:p.Gln138Pro
ENST00000561470.5:c.*459A>C	ENSP00000454267.1:n.*459A>C
ENST00000562606.5:c.503A>C	ENSP00000457020.1:p.Gln168Pro
ENST00000562800.5:c.255+1724A>C	ENSP00000457619.1:n.255+1724A>C
ENST00000563422.5:c.563A>C	ENSP00000457885.1:p.Gln188Pro
ENST00000563786.5:c.503A>C	ENSP00000455241.1:p.Gln168Pro
ENST00000564003.5:c.337+411A>C	ENSP00000454312.1:n.337+411A>C
ENST00000564633.5:c.503A>C	ENSP00000455383.1:p.Gln168Pro
ENST00000565576.5:c.563A>C	ENSP00000454619.1:p.Gln188Pro
ENST00000566377.5:c.563A>C	ENSP00000455405.1:p.Gln188Pro
ENST00000567132.5:c.521A>C	ENSP00000455972.1:p.Gln174Pro
ENST00000567177.1:c.448+411A>C	ENSP00000457013.1:n.448+411A>C
ENST00000568828.5:c.527A>C	ENSP00000455065.1:p.Gln176Pro
ENST00000568907.5:c.473A>C	ENSP00000457494.1:p.Gln158Pro
ENST00000569931.5:c.503A>C	ENSP00000455161.1:p.Gln168Pro
NM_001289155.1:c.563A>C	NP_001276084.1:p.Gln188Pro
NM_001289156.1:c.413A>C	NP_001276085.1:p.Gln138Pro
NM_001289157.1:c.487+411A>C	NP_001276086.1:n.487+411A>C
NM_002435.2:c.563A>C	NP_002426.1:p.Gln188Pro
XM_011521592.1:c.551A>C	XP_011519894.1:p.Gln184Pro
XM_011521593.1:c.503A>C	XP_011519895.1:p.Gln168Pro
NM_001330372.1:c.503A>C	NP_001317301.1:p.Gln168Pro
XM_017022208.1:c.503A>C	XP_016877697.1:p.Gln168Pro
XM_017022209.2:c.413A>C	XP_016877698.1:p.Gln138Pro
NM_002435.3:c.563A>C MANE Select	NP_002426.1:p.Gln188Pro
NM_001289155.2:c.563A>C	NP_001276084.1:p.Gln188Pro
NM_001289156.2:c.413A>C	NP_001276085.1:p.Gln138Pro
NM_001289157.2:c.487+411A>C	NP_001276086.1:n.487+411A>C
NM_001330372.2:c.503A>C	NP_001317301.1:p.Gln168Pro