Canonical Allele Identifier: CA393176155

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188678T>G (hg19) ; chr15:g.74896337T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896337T>G , CM000677.2:g.74896337T>G	GRCh38
NC_000015.9:g.75188678T>G , CM000677.1:g.75188678T>G	GRCh37
NC_000015.8:g.72975731T>G	NCBI36
NG_008921.1:g.11269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+12T>G MANE Select	ENSP00000318318.6:n.844+12T>G
ENST00000323744.10:c.661+12T>G	ENSP00000318192.6:n.661+12T>G
ENST00000352410.8:c.844+12T>G	ENSP00000318318.6:n.844+12T>G
ENST00000535694.5:c.694+12T>G	ENSP00000440447.1:n.694+12T>G
ENST00000562606.5:c.796T>G	ENSP00000457020.1:p.Phe266Val
ENST00000562800.5:c.256-1202T>G	ENSP00000457619.1:n.256-1202T>G
ENST00000563422.5:c.856T>G	ENSP00000457885.1:p.Phe286Val
ENST00000563786.5:c.784+12T>G	ENSP00000455241.1:n.784+12T>G
ENST00000564003.5:c.523T>G	ENSP00000454312.1:p.Phe175Val
ENST00000566377.5:c.844+12T>G	ENSP00000455405.1:n.844+12T>G
ENST00000566556.1:n.904T>G
ENST00000567177.1:c.622+12T>G	ENSP00000457013.1:n.622+12T>G
ENST00000569931.5:c.784+12T>G	ENSP00000455161.1:n.784+12T>G
NM_001289155.1:c.844+12T>G	NP_001276084.1:n.844+12T>G
NM_001289156.1:c.694+12T>G	NP_001276085.1:n.694+12T>G
NM_001289157.1:c.661+12T>G	NP_001276086.1:n.661+12T>G
NM_002435.2:c.844+12T>G	NP_002426.1:n.844+12T>G
XM_011521592.1:c.832+12T>G	XP_011519894.1:n.832+12T>G
XM_011521593.1:c.784+12T>G	XP_011519895.1:n.784+12T>G
NM_001330372.1:c.784+12T>G	NP_001317301.1:n.784+12T>G
XM_017022208.1:c.784+12T>G	XP_016877697.1:n.784+12T>G
XM_017022209.2:c.694+12T>G	XP_016877698.1:n.694+12T>G
NM_002435.3:c.844+12T>G MANE Select	NP_002426.1:n.844+12T>G
NM_001289155.2:c.844+12T>G	NP_001276084.1:n.844+12T>G
NM_001289156.2:c.694+12T>G	NP_001276085.1:n.694+12T>G
NM_001289157.2:c.661+12T>G	NP_001276086.1:n.661+12T>G
NM_001330372.2:c.784+12T>G	NP_001317301.1:n.784+12T>G