Canonical Allele Identifier: CA491491350

Gene: MPI

Linked Data

• gnomAD v4: 15-74896153-G-T
• MyVariant Identifiers: chr15:g.75188494G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896153G>T , CM000677.2:g.74896153G>T	GRCh38
NC_000015.9:g.75188494G>T , CM000677.1:g.75188494G>T	GRCh37
NC_000015.8:g.72975547G>T	NCBI36
NG_008921.1:g.11085G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.672G>T MANE Select	ENSP00000318318.6:p.Ala224=
ENST00000323744.10:c.489G>T	ENSP00000318192.6:p.Thr163=
ENST00000352410.8:c.672G>T	ENSP00000318318.6:p.Ala224=
ENST00000535694.5:c.522G>T	ENSP00000440447.1:p.Ala174=
ENST00000561470.5:c.*568G>T	ENSP00000454267.1:n.*568G>T
ENST00000562606.5:c.612G>T	ENSP00000457020.1:p.Ala204=
ENST00000562800.5:c.256-1386G>T	ENSP00000457619.1:n.256-1386G>T
ENST00000563422.5:c.672G>T	ENSP00000457885.1:p.Ala224=
ENST00000563786.5:c.612G>T	ENSP00000455241.1:p.Ala204=
ENST00000564003.5:c.339G>T	ENSP00000454312.1:p.Thr113=
ENST00000566377.5:c.672G>T	ENSP00000455405.1:p.Ala224=
ENST00000566556.1:n.720G>T
ENST00000567177.1:c.450G>T	ENSP00000457013.1:p.Thr150=
ENST00000569931.5:c.612G>T	ENSP00000455161.1:p.Ala204=
NM_001289155.1:c.672G>T	NP_001276084.1:p.Ala224=
NM_001289156.1:c.522G>T	NP_001276085.1:p.Ala174=
NM_001289157.1:c.489G>T	NP_001276086.1:p.Thr163=
NM_002435.2:c.672G>T	NP_002426.1:p.Ala224=
XM_011521592.1:c.660G>T	XP_011519894.1:p.Ala220=
XM_011521593.1:c.612G>T	XP_011519895.1:p.Ala204=
NM_001330372.1:c.612G>T	NP_001317301.1:p.Ala204=
XM_017022208.1:c.612G>T	XP_016877697.1:p.Ala204=
XM_017022209.2:c.522G>T	XP_016877698.1:p.Ala174=
NM_002435.3:c.672G>T MANE Select	NP_002426.1:p.Ala224=
NM_001289155.2:c.672G>T	NP_001276084.1:p.Ala224=
NM_001289156.2:c.522G>T	NP_001276085.1:p.Ala174=
NM_001289157.2:c.489G>T	NP_001276086.1:p.Thr163=
NM_001330372.2:c.612G>T	NP_001317301.1:p.Ala204=