Canonical Allele Identifier: CA491220364

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75185079C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74892738C>G , CM000677.2:g.74892738C>G	GRCh38
NC_000015.9:g.75185079C>G , CM000677.1:g.75185079C>G	GRCh37
NC_000015.8:g.72972132C>G	NCBI36
NG_008921.1:g.7670C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.423C>G MANE Select	ENSP00000318318.6:p.Ala141=
ENST00000323744.10:c.423C>G	ENSP00000318192.6:p.Ala141=
ENST00000352410.8:c.423C>G	ENSP00000318318.6:p.Ala141=
ENST00000535694.5:c.273C>G	ENSP00000440447.1:p.Ala91=
ENST00000561470.5:c.*319C>G	ENSP00000454267.1:n.*319C>G
ENST00000562606.5:c.363C>G	ENSP00000457020.1:p.Ala121=
ENST00000562800.5:c.255+1249C>G	ENSP00000457619.1:n.255+1249C>G
ENST00000563422.5:c.423C>G	ENSP00000457885.1:p.Ala141=
ENST00000563786.5:c.363C>G	ENSP00000455241.1:p.Ala121=
ENST00000564003.5:c.273C>G	ENSP00000454312.1:p.Ala91=
ENST00000564633.5:c.363C>G	ENSP00000455383.1:p.Ala121=
ENST00000565576.5:c.423C>G	ENSP00000454619.1:p.Ala141=
ENST00000566377.5:c.423C>G	ENSP00000455405.1:p.Ala141=
ENST00000567116.5:n.454C>G
ENST00000567132.5:c.381C>G	ENSP00000455972.1:p.Ala127=
ENST00000567177.1:c.384C>G	ENSP00000457013.1:p.Ala128=
ENST00000568828.5:c.387C>G	ENSP00000455065.1:p.Ala129=
ENST00000568840.1:n.532C>G
ENST00000568907.5:c.333C>G	ENSP00000457494.1:p.Ala111=
ENST00000569233.5:c.480C>G	ENSP00000454622.1:p.Ala160=
ENST00000569931.5:c.363C>G	ENSP00000455161.1:p.Ala121=
NM_001289155.1:c.423C>G	NP_001276084.1:p.Ala141=
NM_001289156.1:c.273C>G	NP_001276085.1:p.Ala91=
NM_001289157.1:c.423C>G	NP_001276086.1:p.Ala141=
NM_002435.2:c.423C>G	NP_002426.1:p.Ala141=
XM_011521592.1:c.411C>G	XP_011519894.1:p.Ala137=
XM_011521593.1:c.363C>G	XP_011519895.1:p.Ala121=
NM_001330372.1:c.363C>G	NP_001317301.1:p.Ala121=
XM_017022208.1:c.363C>G	XP_016877697.1:p.Ala121=
XM_017022209.2:c.273C>G	XP_016877698.1:p.Ala91=
NM_002435.3:c.423C>G MANE Select	NP_002426.1:p.Ala141=
NM_001289155.2:c.423C>G	NP_001276084.1:p.Ala141=
NM_001289156.2:c.273C>G	NP_001276085.1:p.Ala91=
NM_001289157.2:c.423C>G	NP_001276086.1:p.Ala141=
NM_001330372.2:c.363C>G	NP_001317301.1:p.Ala121=