Canonical Allele Identifier: CA7662578

Gene: MPI

Linked Data

• ClinVar Variation Id: 2741820
• ClinVar RCV Id: RCV003516553
• dbSNP Id: rs373478885
• ExAC: 15:75189332 C / T
• gnomAD v2: 15-75189332-C-T
• gnomAD v3: 15-74896991-C-T
• gnomAD v4: 15-74896991-C-T
• MyVariant Identifiers: chr15:g.75189332C>T (hg19) ; chr15:g.74896991C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896991C>T , CM000677.2:g.74896991C>T	GRCh38
NC_000015.9:g.75189332C>T , CM000677.1:g.75189332C>T	GRCh37
NC_000015.8:g.72976385C>T	NCBI36
NG_008921.1:g.11923C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.845-20C>T MANE Select	ENSP00000318318.6:n.845-20C>T
ENST00000323744.10:c.662-20C>T	ENSP00000318192.6:n.662-20C>T
ENST00000352410.8:c.845-20C>T	ENSP00000318318.6:n.845-20C>T
ENST00000535694.5:c.695-20C>T	ENSP00000440447.1:n.695-20C>T
ENST00000562800.5:c.256-548C>T	ENSP00000457619.1:n.256-548C>T
ENST00000563786.5:c.785-20C>T	ENSP00000455241.1:n.785-20C>T
ENST00000566377.5:c.845-521C>T	ENSP00000455405.1:n.845-521C>T
ENST00000566556.1:n.1558C>T
ENST00000567177.1:c.623-521C>T	ENSP00000457013.1:n.623-521C>T
ENST00000569931.5:c.785-20C>T	ENSP00000455161.1:n.785-20C>T
NM_001289155.1:c.845-521C>T	NP_001276084.1:n.845-521C>T
NM_001289156.1:c.695-20C>T	NP_001276085.1:n.695-20C>T
NM_001289157.1:c.662-20C>T	NP_001276086.1:n.662-20C>T
NM_002435.2:c.845-20C>T	NP_002426.1:n.845-20C>T
XM_011521592.1:c.833-20C>T	XP_011519894.1:n.833-20C>T
XM_011521593.1:c.785-20C>T	XP_011519895.1:n.785-20C>T
NM_001330372.1:c.785-20C>T	NP_001317301.1:n.785-20C>T
XM_017022208.1:c.785-521C>T	XP_016877697.1:n.785-521C>T
XM_017022209.2:c.695-521C>T	XP_016877698.1:n.695-521C>T
NM_002435.3:c.845-20C>T MANE Select	NP_002426.1:n.845-20C>T
NM_001289155.2:c.845-521C>T	NP_001276084.1:n.845-521C>T
NM_001289156.2:c.695-20C>T	NP_001276085.1:n.695-20C>T
NM_001289157.2:c.662-20C>T	NP_001276086.1:n.662-20C>T
NM_001330372.2:c.785-20C>T	NP_001317301.1:n.785-20C>T