Canonical Allele Identifier: CA7662664

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897636G>C , CM000677.2:g.74897636G>C	GRCh38
NC_000015.9:g.75189977G>C , CM000677.1:g.75189977G>C	GRCh37
NC_000015.8:g.72977030G>C	NCBI36
NG_008921.1:g.12568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.1178G>C MANE Select	ENSP00000318318.6:p.Gly393Ala
ENST00000323744.10:c.995G>C	ENSP00000318192.6:p.Gly332Ala
ENST00000352410.8:c.1178G>C	ENSP00000318318.6:p.Gly393Ala
ENST00000535694.5:c.1028G>C	ENSP00000440447.1:p.Gly343Ala
ENST00000562800.5:c.353G>C	ENSP00000457619.1:p.Gly118Ala
ENST00000563786.5:c.1118G>C	ENSP00000455241.1:p.Gly373Ala
ENST00000566377.5:c.*105G>C	ENSP00000455405.1:n.*105G>C
ENST00000566556.1:n.2203G>C
ENST00000567177.1:c.747G>C	ENSP00000457013.1:n.747G>C
NM_001289155.1:c.*105G>C	NP_001276084.1:n.*105G>C
NM_001289156.1:c.1028G>C	NP_001276085.1:p.Gly343Ala
NM_001289157.1:c.995G>C	NP_001276086.1:p.Gly332Ala
NM_002435.2:c.1178G>C	NP_002426.1:p.Gly393Ala
XM_011521592.1:c.1166G>C	XP_011519894.1:p.Gly389Ala
XM_011521593.1:c.1118G>C	XP_011519895.1:p.Gly373Ala
NM_001330372.1:c.1118G>C	NP_001317301.1:p.Gly373Ala
XM_017022208.1:c.*105G>C	XP_016877697.1:n.*105G>C
XM_017022209.2:c.*105G>C	XP_016877698.1:n.*105G>C
NM_002435.3:c.1178G>C MANE Select	NP_002426.1:p.Gly393Ala
NM_001289155.2:c.*105G>C	NP_001276084.1:n.*105G>C
NM_001289156.2:c.1028G>C	NP_001276085.1:p.Gly343Ala
NM_001289157.2:c.995G>C	NP_001276086.1:p.Gly332Ala
NM_001330372.2:c.1118G>C	NP_001317301.1:p.Gly373Ala