Canonical Allele Identifier: CA393176142

Gene: MPI

Linked Data

• gnomAD v4: 15-74896332-C-T
• MyVariant Identifiers: chr15:g.75188673C>T (hg19) ; chr15:g.74896332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896332C>T , CM000677.2:g.74896332C>T	GRCh38
NC_000015.9:g.75188673C>T , CM000677.1:g.75188673C>T	GRCh37
NC_000015.8:g.72975726C>T	NCBI36
NG_008921.1:g.11264C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+7C>T MANE Select	ENSP00000318318.6:n.844+7C>T
ENST00000323744.10:c.661+7C>T	ENSP00000318192.6:n.661+7C>T
ENST00000352410.8:c.844+7C>T	ENSP00000318318.6:n.844+7C>T
ENST00000535694.5:c.694+7C>T	ENSP00000440447.1:n.694+7C>T
ENST00000562606.5:c.791C>T	ENSP00000457020.1:p.Pro264Leu
ENST00000562800.5:c.256-1207C>T	ENSP00000457619.1:n.256-1207C>T
ENST00000563422.5:c.851C>T	ENSP00000457885.1:p.Pro284Leu
ENST00000563786.5:c.784+7C>T	ENSP00000455241.1:n.784+7C>T
ENST00000564003.5:c.518C>T	ENSP00000454312.1:p.Pro173Leu
ENST00000566377.5:c.844+7C>T	ENSP00000455405.1:n.844+7C>T
ENST00000566556.1:n.899C>T
ENST00000567177.1:c.622+7C>T	ENSP00000457013.1:n.622+7C>T
ENST00000569931.5:c.784+7C>T	ENSP00000455161.1:n.784+7C>T
NM_001289155.1:c.844+7C>T	NP_001276084.1:n.844+7C>T
NM_001289156.1:c.694+7C>T	NP_001276085.1:n.694+7C>T
NM_001289157.1:c.661+7C>T	NP_001276086.1:n.661+7C>T
NM_002435.2:c.844+7C>T	NP_002426.1:n.844+7C>T
XM_011521592.1:c.832+7C>T	XP_011519894.1:n.832+7C>T
XM_011521593.1:c.784+7C>T	XP_011519895.1:n.784+7C>T
NM_001330372.1:c.784+7C>T	NP_001317301.1:n.784+7C>T
XM_017022208.1:c.784+7C>T	XP_016877697.1:n.784+7C>T
XM_017022209.2:c.694+7C>T	XP_016877698.1:n.694+7C>T
NM_002435.3:c.844+7C>T MANE Select	NP_002426.1:n.844+7C>T
NM_001289155.2:c.844+7C>T	NP_001276084.1:n.844+7C>T
NM_001289156.2:c.694+7C>T	NP_001276085.1:n.694+7C>T
NM_001289157.2:c.661+7C>T	NP_001276086.1:n.661+7C>T
NM_001330372.2:c.784+7C>T	NP_001317301.1:n.784+7C>T