Canonical Allele Identifier: CA2629530095

Gene: MPI

Linked Data

• gnomAD v4: 15-74896010-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896010G>C , CM000677.2:g.74896010G>C	GRCh38
NC_000015.9:g.75188351G>C , CM000677.1:g.75188351G>C	GRCh37
NC_000015.8:g.72975404G>C	NCBI36
NG_008921.1:g.10942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.671-142G>C MANE Select	ENSP00000318318.6:n.671-142G>C
ENST00000323744.10:c.488-142G>C	ENSP00000318192.6:n.488-142G>C
ENST00000352410.8:c.671-142G>C	ENSP00000318318.6:n.671-142G>C
ENST00000535694.5:c.521-142G>C	ENSP00000440447.1:n.521-142G>C
ENST00000561470.5:c.*567-142G>C	ENSP00000454267.1:n.*567-142G>C
ENST00000562606.5:c.611-142G>C	ENSP00000457020.1:n.611-142G>C
ENST00000562800.5:c.256-1529G>C	ENSP00000457619.1:n.256-1529G>C
ENST00000563422.5:c.671-142G>C	ENSP00000457885.1:n.671-142G>C
ENST00000563786.5:c.611-142G>C	ENSP00000455241.1:n.611-142G>C
ENST00000564003.5:c.338-142G>C	ENSP00000454312.1:n.338-142G>C
ENST00000566377.5:c.671-142G>C	ENSP00000455405.1:n.671-142G>C
ENST00000566556.1:n.577G>C
ENST00000567177.1:c.449-142G>C	ENSP00000457013.1:n.449-142G>C
ENST00000569931.5:c.611-142G>C	ENSP00000455161.1:n.611-142G>C
NM_001289155.1:c.671-142G>C	NP_001276084.1:n.671-142G>C
NM_001289156.1:c.521-142G>C	NP_001276085.1:n.521-142G>C
NM_001289157.1:c.488-142G>C	NP_001276086.1:n.488-142G>C
NM_002435.2:c.671-142G>C	NP_002426.1:n.671-142G>C
XM_011521592.1:c.659-142G>C	XP_011519894.1:n.659-142G>C
XM_011521593.1:c.611-142G>C	XP_011519895.1:n.611-142G>C
NM_001330372.1:c.611-142G>C	NP_001317301.1:n.611-142G>C
XM_017022208.1:c.611-142G>C	XP_016877697.1:n.611-142G>C
XM_017022209.2:c.521-142G>C	XP_016877698.1:n.521-142G>C
NM_002435.3:c.671-142G>C MANE Select	NP_002426.1:n.671-142G>C
NM_001289155.2:c.671-142G>C	NP_001276084.1:n.671-142G>C
NM_001289156.2:c.521-142G>C	NP_001276085.1:n.521-142G>C
NM_001289157.2:c.488-142G>C	NP_001276086.1:n.488-142G>C
NM_001330372.2:c.611-142G>C	NP_001317301.1:n.611-142G>C