Canonical Allele Identifier: CA7662581

Gene: MPI

Linked Data

• ClinVar Variation Id: 1923885
• ClinVar RCV Id: RCV002609208
• dbSNP Id: rs749734985
• ExAC: 15:75189335 G / T
• gnomAD v2: 15-75189335-G-T
• gnomAD v3: 15-74896994-G-T
• gnomAD v4: 15-74896994-G-T
• MyVariant Identifiers: chr15:g.75189335G>T (hg19) ; chr15:g.74896994G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896994G>T , CM000677.2:g.74896994G>T	GRCh38
NC_000015.9:g.75189335G>T , CM000677.1:g.75189335G>T	GRCh37
NC_000015.8:g.72976388G>T	NCBI36
NG_008921.1:g.11926G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.845-17G>T MANE Select	ENSP00000318318.6:n.845-17G>T
ENST00000323744.10:c.662-17G>T	ENSP00000318192.6:n.662-17G>T
ENST00000352410.8:c.845-17G>T	ENSP00000318318.6:n.845-17G>T
ENST00000535694.5:c.695-17G>T	ENSP00000440447.1:n.695-17G>T
ENST00000562800.5:c.256-545G>T	ENSP00000457619.1:n.256-545G>T
ENST00000563786.5:c.785-17G>T	ENSP00000455241.1:n.785-17G>T
ENST00000566377.5:c.845-518G>T	ENSP00000455405.1:n.845-518G>T
ENST00000566556.1:n.1561G>T
ENST00000567177.1:c.623-518G>T	ENSP00000457013.1:n.623-518G>T
ENST00000569931.5:c.785-17G>T	ENSP00000455161.1:n.785-17G>T
NM_001289155.1:c.845-518G>T	NP_001276084.1:n.845-518G>T
NM_001289156.1:c.695-17G>T	NP_001276085.1:n.695-17G>T
NM_001289157.1:c.662-17G>T	NP_001276086.1:n.662-17G>T
NM_002435.2:c.845-17G>T	NP_002426.1:n.845-17G>T
XM_011521592.1:c.833-17G>T	XP_011519894.1:n.833-17G>T
XM_011521593.1:c.785-17G>T	XP_011519895.1:n.785-17G>T
NM_001330372.1:c.785-17G>T	NP_001317301.1:n.785-17G>T
XM_017022208.1:c.785-518G>T	XP_016877697.1:n.785-518G>T
XM_017022209.2:c.695-518G>T	XP_016877698.1:n.695-518G>T
NM_002435.3:c.845-17G>T MANE Select	NP_002426.1:n.845-17G>T
NM_001289155.2:c.845-518G>T	NP_001276084.1:n.845-518G>T
NM_001289156.2:c.695-17G>T	NP_001276085.1:n.695-17G>T
NM_001289157.2:c.662-17G>T	NP_001276086.1:n.662-17G>T
NM_001330372.2:c.785-17G>T	NP_001317301.1:n.785-17G>T