Canonical Allele Identifier: CA491491467

Gene: MPI

Linked Data

• ClinVar Variation Id: 2849939
• ClinVar RCV Id: RCV003630866
• gnomAD v4: 15-74896315-C-T
• MyVariant Identifiers: chr15:g.75188656C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896315C>T , CM000677.2:g.74896315C>T	GRCh38
NC_000015.9:g.75188656C>T , CM000677.1:g.75188656C>T	GRCh37
NC_000015.8:g.72975709C>T	NCBI36
NG_008921.1:g.11247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.834C>T MANE Select	ENSP00000318318.6:p.Tyr278=
ENST00000323744.10:c.651C>T	ENSP00000318192.6:p.Tyr217=
ENST00000352410.8:c.834C>T	ENSP00000318318.6:p.Tyr278=
ENST00000535694.5:c.684C>T	ENSP00000440447.1:p.Tyr228=
ENST00000562606.5:c.774C>T	ENSP00000457020.1:p.Tyr258=
ENST00000562800.5:c.256-1224C>T	ENSP00000457619.1:n.256-1224C>T
ENST00000563422.5:c.834C>T	ENSP00000457885.1:p.Tyr278=
ENST00000563786.5:c.774C>T	ENSP00000455241.1:p.Tyr258=
ENST00000564003.5:c.501C>T	ENSP00000454312.1:p.Tyr167=
ENST00000566377.5:c.834C>T	ENSP00000455405.1:p.Tyr278=
ENST00000566556.1:n.882C>T
ENST00000567177.1:c.612C>T	ENSP00000457013.1:p.Tyr204=
ENST00000569931.5:c.774C>T	ENSP00000455161.1:p.Tyr258=
NM_001289155.1:c.834C>T	NP_001276084.1:p.Tyr278=
NM_001289156.1:c.684C>T	NP_001276085.1:p.Tyr228=
NM_001289157.1:c.651C>T	NP_001276086.1:p.Tyr217=
NM_002435.2:c.834C>T	NP_002426.1:p.Tyr278=
XM_011521592.1:c.822C>T	XP_011519894.1:p.Tyr274=
XM_011521593.1:c.774C>T	XP_011519895.1:p.Tyr258=
NM_001330372.1:c.774C>T	NP_001317301.1:p.Tyr258=
XM_017022208.1:c.774C>T	XP_016877697.1:p.Tyr258=
XM_017022209.2:c.684C>T	XP_016877698.1:p.Tyr228=
NM_002435.3:c.834C>T MANE Select	NP_002426.1:p.Tyr278=
NM_001289155.2:c.834C>T	NP_001276084.1:p.Tyr278=
NM_001289156.2:c.684C>T	NP_001276085.1:p.Tyr228=
NM_001289157.2:c.651C>T	NP_001276086.1:p.Tyr217=
NM_001330372.2:c.774C>T	NP_001317301.1:p.Tyr258=