Canonical Allele Identifier: CA393177328

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75189397G>A (hg19) ; chr15:g.74897056G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897056G>A , CM000677.2:g.74897056G>A	GRCh38
NC_000015.9:g.75189397G>A , CM000677.1:g.75189397G>A	GRCh37
NC_000015.8:g.72976450G>A	NCBI36
NG_008921.1:g.11988G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.890G>A MANE Select	ENSP00000318318.6:p.Gly297Asp
ENST00000323744.10:c.707G>A	ENSP00000318192.6:p.Gly236Asp
ENST00000352410.8:c.890G>A	ENSP00000318318.6:p.Gly297Asp
ENST00000535694.5:c.740G>A	ENSP00000440447.1:p.Gly247Asp
ENST00000562800.5:c.256-483G>A	ENSP00000457619.1:n.256-483G>A
ENST00000563786.5:c.830G>A	ENSP00000455241.1:p.Gly277Asp
ENST00000566377.5:c.845-456G>A	ENSP00000455405.1:n.845-456G>A
ENST00000566556.1:n.1623G>A
ENST00000567177.1:c.623-456G>A	ENSP00000457013.1:n.623-456G>A
ENST00000569931.5:c.830G>A	ENSP00000455161.1:p.Gly277Asp
NM_001289155.1:c.845-456G>A	NP_001276084.1:n.845-456G>A
NM_001289156.1:c.740G>A	NP_001276085.1:p.Gly247Asp
NM_001289157.1:c.707G>A	NP_001276086.1:p.Gly236Asp
NM_002435.2:c.890G>A	NP_002426.1:p.Gly297Asp
XM_011521592.1:c.878G>A	XP_011519894.1:p.Gly293Asp
XM_011521593.1:c.830G>A	XP_011519895.1:p.Gly277Asp
NM_001330372.1:c.830G>A	NP_001317301.1:p.Gly277Asp
XM_017022208.1:c.785-456G>A	XP_016877697.1:n.785-456G>A
XM_017022209.2:c.695-456G>A	XP_016877698.1:n.695-456G>A
NM_002435.3:c.890G>A MANE Select	NP_002426.1:p.Gly297Asp
NM_001289155.2:c.845-456G>A	NP_001276084.1:n.845-456G>A
NM_001289156.2:c.740G>A	NP_001276085.1:p.Gly247Asp
NM_001289157.2:c.707G>A	NP_001276086.1:p.Gly236Asp
NM_001330372.2:c.830G>A	NP_001317301.1:p.Gly277Asp