Canonical Allele Identifier: CA491491454

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188647C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896306C>G , CM000677.2:g.74896306C>G	GRCh38
NC_000015.9:g.75188647C>G , CM000677.1:g.75188647C>G	GRCh37
NC_000015.8:g.72975700C>G	NCBI36
NG_008921.1:g.11238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.825C>G MANE Select	ENSP00000318318.6:p.Pro275=
ENST00000323744.10:c.642C>G	ENSP00000318192.6:p.Pro214=
ENST00000352410.8:c.825C>G	ENSP00000318318.6:p.Pro275=
ENST00000535694.5:c.675C>G	ENSP00000440447.1:p.Pro225=
ENST00000562606.5:c.765C>G	ENSP00000457020.1:p.Pro255=
ENST00000562800.5:c.256-1233C>G	ENSP00000457619.1:n.256-1233C>G
ENST00000563422.5:c.825C>G	ENSP00000457885.1:p.Pro275=
ENST00000563786.5:c.765C>G	ENSP00000455241.1:p.Pro255=
ENST00000564003.5:c.492C>G	ENSP00000454312.1:p.Pro164=
ENST00000566377.5:c.825C>G	ENSP00000455405.1:p.Pro275=
ENST00000566556.1:n.873C>G
ENST00000567177.1:c.603C>G	ENSP00000457013.1:p.Pro201=
ENST00000569931.5:c.765C>G	ENSP00000455161.1:p.Pro255=
NM_001289155.1:c.825C>G	NP_001276084.1:p.Pro275=
NM_001289156.1:c.675C>G	NP_001276085.1:p.Pro225=
NM_001289157.1:c.642C>G	NP_001276086.1:p.Pro214=
NM_002435.2:c.825C>G	NP_002426.1:p.Pro275=
XM_011521592.1:c.813C>G	XP_011519894.1:p.Pro271=
XM_011521593.1:c.765C>G	XP_011519895.1:p.Pro255=
NM_001330372.1:c.765C>G	NP_001317301.1:p.Pro255=
XM_017022208.1:c.765C>G	XP_016877697.1:p.Pro255=
XM_017022209.2:c.675C>G	XP_016877698.1:p.Pro225=
NM_002435.3:c.825C>G MANE Select	NP_002426.1:p.Pro275=
NM_001289155.2:c.825C>G	NP_001276084.1:p.Pro275=
NM_001289156.2:c.675C>G	NP_001276085.1:p.Pro225=
NM_001289157.2:c.642C>G	NP_001276086.1:p.Pro214=
NM_001330372.2:c.765C>G	NP_001317301.1:p.Pro255=