Canonical Allele Identifier: CA393175896
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74896215A>T , CM000677.2:g.74896215A>T GRCh38
NC_000015.9:g.75188556A>T , CM000677.1:g.75188556A>T GRCh37
NC_000015.8:g.72975609A>T NCBI36
NG_008921.1:g.11147A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.734A>T MANE Select ENSP00000318318.6:p.Tyr245Phe
ENST00000323744.10:c.551A>T ENSP00000318192.6:p.Tyr184Phe
ENST00000352410.8:c.734A>T ENSP00000318318.6:p.Tyr245Phe
ENST00000535694.5:c.584A>T ENSP00000440447.1:p.Tyr195Phe
ENST00000562606.5:c.674A>T ENSP00000457020.1:p.Tyr225Phe
ENST00000562800.5:c.256-1324A>T ENSP00000457619.1:n.256-1324A>T
ENST00000563422.5:c.734A>T ENSP00000457885.1:p.Tyr245Phe
ENST00000563786.5:c.674A>T ENSP00000455241.1:p.Tyr225Phe
ENST00000564003.5:c.401A>T ENSP00000454312.1:p.Tyr134Phe
ENST00000566377.5:c.734A>T ENSP00000455405.1:p.Tyr245Phe
ENST00000566556.1:n.782A>T
ENST00000567177.1:c.512A>T ENSP00000457013.1:p.Tyr171Phe
ENST00000569931.5:c.674A>T ENSP00000455161.1:p.Tyr225Phe
NM_001289155.1:c.734A>T NP_001276084.1:p.Tyr245Phe
NM_001289156.1:c.584A>T NP_001276085.1:p.Tyr195Phe
NM_001289157.1:c.551A>T NP_001276086.1:p.Tyr184Phe
NM_002435.2:c.734A>T NP_002426.1:p.Tyr245Phe
XM_011521592.1:c.722A>T XP_011519894.1:p.Tyr241Phe
XM_011521593.1:c.674A>T XP_011519895.1:p.Tyr225Phe
NM_001330372.1:c.674A>T NP_001317301.1:p.Tyr225Phe
XM_017022208.1:c.674A>T XP_016877697.1:p.Tyr225Phe
XM_017022209.2:c.584A>T XP_016877698.1:p.Tyr195Phe
NM_002435.3:c.734A>T MANE Select NP_002426.1:p.Tyr245Phe
NM_001289155.2:c.734A>T NP_001276084.1:p.Tyr245Phe
NM_001289156.2:c.584A>T NP_001276085.1:p.Tyr195Phe
NM_001289157.2:c.551A>T NP_001276086.1:p.Tyr184Phe
NM_001330372.2:c.674A>T NP_001317301.1:p.Tyr225Phe