Canonical Allele Identifier: CA393177367

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75189403C>G (hg19) ; chr15:g.74897062C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897062C>G , CM000677.2:g.74897062C>G	GRCh38
NC_000015.9:g.75189403C>G , CM000677.1:g.75189403C>G	GRCh37
NC_000015.8:g.72976456C>G	NCBI36
NG_008921.1:g.11994C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.896C>G MANE Select	ENSP00000318318.6:p.Thr299Arg
ENST00000323744.10:c.713C>G	ENSP00000318192.6:p.Thr238Arg
ENST00000352410.8:c.896C>G	ENSP00000318318.6:p.Thr299Arg
ENST00000535694.5:c.746C>G	ENSP00000440447.1:p.Thr249Arg
ENST00000562800.5:c.256-477C>G	ENSP00000457619.1:n.256-477C>G
ENST00000563786.5:c.836C>G	ENSP00000455241.1:p.Thr279Arg
ENST00000566377.5:c.845-450C>G	ENSP00000455405.1:n.845-450C>G
ENST00000566556.1:n.1629C>G
ENST00000567177.1:c.623-450C>G	ENSP00000457013.1:n.623-450C>G
ENST00000569931.5:c.836C>G	ENSP00000455161.1:p.Thr279Arg
NM_001289155.1:c.845-450C>G	NP_001276084.1:n.845-450C>G
NM_001289156.1:c.746C>G	NP_001276085.1:p.Thr249Arg
NM_001289157.1:c.713C>G	NP_001276086.1:p.Thr238Arg
NM_002435.2:c.896C>G	NP_002426.1:p.Thr299Arg
XM_011521592.1:c.884C>G	XP_011519894.1:p.Thr295Arg
XM_011521593.1:c.836C>G	XP_011519895.1:p.Thr279Arg
NM_001330372.1:c.836C>G	NP_001317301.1:p.Thr279Arg
XM_017022208.1:c.785-450C>G	XP_016877697.1:n.785-450C>G
XM_017022209.2:c.695-450C>G	XP_016877698.1:n.695-450C>G
NM_002435.3:c.896C>G MANE Select	NP_002426.1:p.Thr299Arg
NM_001289155.2:c.845-450C>G	NP_001276084.1:n.845-450C>G
NM_001289156.2:c.746C>G	NP_001276085.1:p.Thr249Arg
NM_001289157.2:c.713C>G	NP_001276086.1:p.Thr238Arg
NM_001330372.2:c.836C>G	NP_001317301.1:p.Thr279Arg