Canonical Allele Identifier: CA393177360

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75189402A>C (hg19) ; chr15:g.74897061A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897061A>C , CM000677.2:g.74897061A>C	GRCh38
NC_000015.9:g.75189402A>C , CM000677.1:g.75189402A>C	GRCh37
NC_000015.8:g.72976455A>C	NCBI36
NG_008921.1:g.11993A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.895A>C MANE Select	ENSP00000318318.6:p.Thr299Pro
ENST00000323744.10:c.712A>C	ENSP00000318192.6:p.Thr238Pro
ENST00000352410.8:c.895A>C	ENSP00000318318.6:p.Thr299Pro
ENST00000535694.5:c.745A>C	ENSP00000440447.1:p.Thr249Pro
ENST00000562800.5:c.256-478A>C	ENSP00000457619.1:n.256-478A>C
ENST00000563786.5:c.835A>C	ENSP00000455241.1:p.Thr279Pro
ENST00000566377.5:c.845-451A>C	ENSP00000455405.1:n.845-451A>C
ENST00000566556.1:n.1628A>C
ENST00000567177.1:c.623-451A>C	ENSP00000457013.1:n.623-451A>C
ENST00000569931.5:c.835A>C	ENSP00000455161.1:p.Thr279Pro
NM_001289155.1:c.845-451A>C	NP_001276084.1:n.845-451A>C
NM_001289156.1:c.745A>C	NP_001276085.1:p.Thr249Pro
NM_001289157.1:c.712A>C	NP_001276086.1:p.Thr238Pro
NM_002435.2:c.895A>C	NP_002426.1:p.Thr299Pro
XM_011521592.1:c.883A>C	XP_011519894.1:p.Thr295Pro
XM_011521593.1:c.835A>C	XP_011519895.1:p.Thr279Pro
NM_001330372.1:c.835A>C	NP_001317301.1:p.Thr279Pro
XM_017022208.1:c.785-451A>C	XP_016877697.1:n.785-451A>C
XM_017022209.2:c.695-451A>C	XP_016877698.1:n.695-451A>C
NM_002435.3:c.895A>C MANE Select	NP_002426.1:p.Thr299Pro
NM_001289155.2:c.845-451A>C	NP_001276084.1:n.845-451A>C
NM_001289156.2:c.745A>C	NP_001276085.1:p.Thr249Pro
NM_001289157.2:c.712A>C	NP_001276086.1:p.Thr238Pro
NM_001330372.2:c.835A>C	NP_001317301.1:p.Thr279Pro