Canonical Allele Identifier: CA491220515

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75189404A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897063A>C , CM000677.2:g.74897063A>C	GRCh38
NC_000015.9:g.75189404A>C , CM000677.1:g.75189404A>C	GRCh37
NC_000015.8:g.72976457A>C	NCBI36
NG_008921.1:g.11995A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.897A>C MANE Select	ENSP00000318318.6:p.Thr299=
ENST00000323744.10:c.714A>C	ENSP00000318192.6:p.Thr238=
ENST00000352410.8:c.897A>C	ENSP00000318318.6:p.Thr299=
ENST00000535694.5:c.747A>C	ENSP00000440447.1:p.Thr249=
ENST00000562800.5:c.256-476A>C	ENSP00000457619.1:n.256-476A>C
ENST00000563786.5:c.837A>C	ENSP00000455241.1:p.Thr279=
ENST00000566377.5:c.845-449A>C	ENSP00000455405.1:n.845-449A>C
ENST00000566556.1:n.1630A>C
ENST00000567177.1:c.623-449A>C	ENSP00000457013.1:n.623-449A>C
ENST00000569931.5:c.837A>C	ENSP00000455161.1:p.Thr279=
NM_001289155.1:c.845-449A>C	NP_001276084.1:n.845-449A>C
NM_001289156.1:c.747A>C	NP_001276085.1:p.Thr249=
NM_001289157.1:c.714A>C	NP_001276086.1:p.Thr238=
NM_002435.2:c.897A>C	NP_002426.1:p.Thr299=
XM_011521592.1:c.885A>C	XP_011519894.1:p.Thr295=
XM_011521593.1:c.837A>C	XP_011519895.1:p.Thr279=
NM_001330372.1:c.837A>C	NP_001317301.1:p.Thr279=
XM_017022208.1:c.785-449A>C	XP_016877697.1:n.785-449A>C
XM_017022209.2:c.695-449A>C	XP_016877698.1:n.695-449A>C
NM_002435.3:c.897A>C MANE Select	NP_002426.1:p.Thr299=
NM_001289155.2:c.845-449A>C	NP_001276084.1:n.845-449A>C
NM_001289156.2:c.747A>C	NP_001276085.1:p.Thr249=
NM_001289157.2:c.714A>C	NP_001276086.1:p.Thr238=
NM_001330372.2:c.837A>C	NP_001317301.1:p.Thr279=