Canonical Allele Identifier: CA393176021

Gene: MPI

Linked Data

• COSMIC: COSM75452
• MyVariant Identifiers: chr15:g.75188616G>T (hg19) ; chr15:g.74896275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896275G>T , CM000677.2:g.74896275G>T	GRCh38
NC_000015.9:g.75188616G>T , CM000677.1:g.75188616G>T	GRCh37
NC_000015.8:g.72975669G>T	NCBI36
NG_008921.1:g.11207G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.794G>T MANE Select	ENSP00000318318.6:p.Gly265Val
ENST00000323744.10:c.611G>T	ENSP00000318192.6:p.Gly204Val
ENST00000352410.8:c.794G>T	ENSP00000318318.6:p.Gly265Val
ENST00000535694.5:c.644G>T	ENSP00000440447.1:p.Gly215Val
ENST00000562606.5:c.734G>T	ENSP00000457020.1:p.Gly245Val
ENST00000562800.5:c.256-1264G>T	ENSP00000457619.1:n.256-1264G>T
ENST00000563422.5:c.794G>T	ENSP00000457885.1:p.Gly265Val
ENST00000563786.5:c.734G>T	ENSP00000455241.1:p.Gly245Val
ENST00000564003.5:c.461G>T	ENSP00000454312.1:p.Gly154Val
ENST00000566377.5:c.794G>T	ENSP00000455405.1:p.Gly265Val
ENST00000566556.1:n.842G>T
ENST00000567177.1:c.572G>T	ENSP00000457013.1:p.Gly191Val
ENST00000569931.5:c.734G>T	ENSP00000455161.1:p.Gly245Val
NM_001289155.1:c.794G>T	NP_001276084.1:p.Gly265Val
NM_001289156.1:c.644G>T	NP_001276085.1:p.Gly215Val
NM_001289157.1:c.611G>T	NP_001276086.1:p.Gly204Val
NM_002435.2:c.794G>T	NP_002426.1:p.Gly265Val
XM_011521592.1:c.782G>T	XP_011519894.1:p.Gly261Val
XM_011521593.1:c.734G>T	XP_011519895.1:p.Gly245Val
NM_001330372.1:c.734G>T	NP_001317301.1:p.Gly245Val
XM_017022208.1:c.734G>T	XP_016877697.1:p.Gly245Val
XM_017022209.2:c.644G>T	XP_016877698.1:p.Gly215Val
NM_002435.3:c.794G>T MANE Select	NP_002426.1:p.Gly265Val
NM_001289155.2:c.794G>T	NP_001276084.1:p.Gly265Val
NM_001289156.2:c.644G>T	NP_001276085.1:p.Gly215Val
NM_001289157.2:c.611G>T	NP_001276086.1:p.Gly204Val
NM_001330372.2:c.734G>T	NP_001317301.1:p.Gly245Val