Canonical Allele Identifier: CA491491478

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188662A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896321A>G , CM000677.2:g.74896321A>G	GRCh38
NC_000015.9:g.75188662A>G , CM000677.1:g.75188662A>G	GRCh37
NC_000015.8:g.72975715A>G	NCBI36
NG_008921.1:g.11253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.840A>G MANE Select	ENSP00000318318.6:p.Lys280=
ENST00000323744.10:c.657A>G	ENSP00000318192.6:p.Lys219=
ENST00000352410.8:c.840A>G	ENSP00000318318.6:p.Lys280=
ENST00000535694.5:c.690A>G	ENSP00000440447.1:p.Lys230=
ENST00000562606.5:c.780A>G	ENSP00000457020.1:p.Lys260=
ENST00000562800.5:c.256-1218A>G	ENSP00000457619.1:n.256-1218A>G
ENST00000563422.5:c.840A>G	ENSP00000457885.1:p.Lys280=
ENST00000563786.5:c.780A>G	ENSP00000455241.1:p.Lys260=
ENST00000564003.5:c.507A>G	ENSP00000454312.1:p.Lys169=
ENST00000566377.5:c.840A>G	ENSP00000455405.1:p.Lys280=
ENST00000566556.1:n.888A>G
ENST00000567177.1:c.618A>G	ENSP00000457013.1:p.Lys206=
ENST00000569931.5:c.780A>G	ENSP00000455161.1:p.Lys260=
NM_001289155.1:c.840A>G	NP_001276084.1:p.Lys280=
NM_001289156.1:c.690A>G	NP_001276085.1:p.Lys230=
NM_001289157.1:c.657A>G	NP_001276086.1:p.Lys219=
NM_002435.2:c.840A>G	NP_002426.1:p.Lys280=
XM_011521592.1:c.828A>G	XP_011519894.1:p.Lys276=
XM_011521593.1:c.780A>G	XP_011519895.1:p.Lys260=
NM_001330372.1:c.780A>G	NP_001317301.1:p.Lys260=
XM_017022208.1:c.780A>G	XP_016877697.1:p.Lys260=
XM_017022209.2:c.690A>G	XP_016877698.1:p.Lys230=
NM_002435.3:c.840A>G MANE Select	NP_002426.1:p.Lys280=
NM_001289155.2:c.840A>G	NP_001276084.1:p.Lys280=
NM_001289156.2:c.690A>G	NP_001276085.1:p.Lys230=
NM_001289157.2:c.657A>G	NP_001276086.1:p.Lys219=
NM_001330372.2:c.780A>G	NP_001317301.1:p.Lys260=