Canonical Allele Identifier: CA393176079

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188643T>C (hg19) ; chr15:g.74896302T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896302T>C , CM000677.2:g.74896302T>C	GRCh38
NC_000015.9:g.75188643T>C , CM000677.1:g.75188643T>C	GRCh37
NC_000015.8:g.72975696T>C	NCBI36
NG_008921.1:g.11234T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.821T>C MANE Select	ENSP00000318318.6:p.Val274Ala
ENST00000323744.10:c.638T>C	ENSP00000318192.6:p.Val213Ala
ENST00000352410.8:c.821T>C	ENSP00000318318.6:p.Val274Ala
ENST00000535694.5:c.671T>C	ENSP00000440447.1:p.Val224Ala
ENST00000562606.5:c.761T>C	ENSP00000457020.1:p.Val254Ala
ENST00000562800.5:c.256-1237T>C	ENSP00000457619.1:n.256-1237T>C
ENST00000563422.5:c.821T>C	ENSP00000457885.1:p.Val274Ala
ENST00000563786.5:c.761T>C	ENSP00000455241.1:p.Val254Ala
ENST00000564003.5:c.488T>C	ENSP00000454312.1:p.Val163Ala
ENST00000566377.5:c.821T>C	ENSP00000455405.1:p.Val274Ala
ENST00000566556.1:n.869T>C
ENST00000567177.1:c.599T>C	ENSP00000457013.1:p.Val200Ala
ENST00000569931.5:c.761T>C	ENSP00000455161.1:p.Val254Ala
NM_001289155.1:c.821T>C	NP_001276084.1:p.Val274Ala
NM_001289156.1:c.671T>C	NP_001276085.1:p.Val224Ala
NM_001289157.1:c.638T>C	NP_001276086.1:p.Val213Ala
NM_002435.2:c.821T>C	NP_002426.1:p.Val274Ala
XM_011521592.1:c.809T>C	XP_011519894.1:p.Val270Ala
XM_011521593.1:c.761T>C	XP_011519895.1:p.Val254Ala
NM_001330372.1:c.761T>C	NP_001317301.1:p.Val254Ala
XM_017022208.1:c.761T>C	XP_016877697.1:p.Val254Ala
XM_017022209.2:c.671T>C	XP_016877698.1:p.Val224Ala
NM_002435.3:c.821T>C MANE Select	NP_002426.1:p.Val274Ala
NM_001289155.2:c.821T>C	NP_001276084.1:p.Val274Ala
NM_001289156.2:c.671T>C	NP_001276085.1:p.Val224Ala
NM_001289157.2:c.638T>C	NP_001276086.1:p.Val213Ala
NM_001330372.2:c.761T>C	NP_001317301.1:p.Val254Ala