Canonical Allele Identifier: CA393177371

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75189405C>A (hg19) ; chr15:g.74897064C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897064C>A , CM000677.2:g.74897064C>A	GRCh38
NC_000015.9:g.75189405C>A , CM000677.1:g.75189405C>A	GRCh37
NC_000015.8:g.72976458C>A	NCBI36
NG_008921.1:g.11996C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.898C>A MANE Select	ENSP00000318318.6:p.Pro300Thr
ENST00000323744.10:c.715C>A	ENSP00000318192.6:p.Pro239Thr
ENST00000352410.8:c.898C>A	ENSP00000318318.6:p.Pro300Thr
ENST00000535694.5:c.748C>A	ENSP00000440447.1:p.Pro250Thr
ENST00000562800.5:c.256-475C>A	ENSP00000457619.1:n.256-475C>A
ENST00000563786.5:c.838C>A	ENSP00000455241.1:p.Pro280Thr
ENST00000566377.5:c.845-448C>A	ENSP00000455405.1:n.845-448C>A
ENST00000566556.1:n.1631C>A
ENST00000567177.1:c.623-448C>A	ENSP00000457013.1:n.623-448C>A
ENST00000569931.5:c.838C>A	ENSP00000455161.1:p.Pro280Thr
NM_001289155.1:c.845-448C>A	NP_001276084.1:n.845-448C>A
NM_001289156.1:c.748C>A	NP_001276085.1:p.Pro250Thr
NM_001289157.1:c.715C>A	NP_001276086.1:p.Pro239Thr
NM_002435.2:c.898C>A	NP_002426.1:p.Pro300Thr
XM_011521592.1:c.886C>A	XP_011519894.1:p.Pro296Thr
XM_011521593.1:c.838C>A	XP_011519895.1:p.Pro280Thr
NM_001330372.1:c.838C>A	NP_001317301.1:p.Pro280Thr
XM_017022208.1:c.785-448C>A	XP_016877697.1:n.785-448C>A
XM_017022209.2:c.695-448C>A	XP_016877698.1:n.695-448C>A
NM_002435.3:c.898C>A MANE Select	NP_002426.1:p.Pro300Thr
NM_001289155.2:c.845-448C>A	NP_001276084.1:n.845-448C>A
NM_001289156.2:c.748C>A	NP_001276085.1:p.Pro250Thr
NM_001289157.2:c.715C>A	NP_001276086.1:p.Pro239Thr
NM_001330372.2:c.838C>A	NP_001317301.1:p.Pro280Thr