Canonical Allele Identifier: CA393176075

Gene: MPI

Linked Data

• MyVariant Identifiers: chr15:g.75188641C>A (hg19) ; chr15:g.74896300C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896300C>A , CM000677.2:g.74896300C>A	GRCh38
NC_000015.9:g.75188641C>A , CM000677.1:g.75188641C>A	GRCh37
NC_000015.8:g.72975694C>A	NCBI36
NG_008921.1:g.11232C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.819C>A MANE Select	ENSP00000318318.6:p.Asn273Lys
ENST00000323744.10:c.636C>A	ENSP00000318192.6:p.Asn212Lys
ENST00000352410.8:c.819C>A	ENSP00000318318.6:p.Asn273Lys
ENST00000535694.5:c.669C>A	ENSP00000440447.1:p.Asn223Lys
ENST00000562606.5:c.759C>A	ENSP00000457020.1:p.Asn253Lys
ENST00000562800.5:c.256-1239C>A	ENSP00000457619.1:n.256-1239C>A
ENST00000563422.5:c.819C>A	ENSP00000457885.1:p.Asn273Lys
ENST00000563786.5:c.759C>A	ENSP00000455241.1:p.Asn253Lys
ENST00000564003.5:c.486C>A	ENSP00000454312.1:p.Asn162Lys
ENST00000566377.5:c.819C>A	ENSP00000455405.1:p.Asn273Lys
ENST00000566556.1:n.867C>A
ENST00000567177.1:c.597C>A	ENSP00000457013.1:p.Asn199Lys
ENST00000569931.5:c.759C>A	ENSP00000455161.1:p.Asn253Lys
NM_001289155.1:c.819C>A	NP_001276084.1:p.Asn273Lys
NM_001289156.1:c.669C>A	NP_001276085.1:p.Asn223Lys
NM_001289157.1:c.636C>A	NP_001276086.1:p.Asn212Lys
NM_002435.2:c.819C>A	NP_002426.1:p.Asn273Lys
XM_011521592.1:c.807C>A	XP_011519894.1:p.Asn269Lys
XM_011521593.1:c.759C>A	XP_011519895.1:p.Asn253Lys
NM_001330372.1:c.759C>A	NP_001317301.1:p.Asn253Lys
XM_017022208.1:c.759C>A	XP_016877697.1:p.Asn253Lys
XM_017022209.2:c.669C>A	XP_016877698.1:p.Asn223Lys
NM_002435.3:c.819C>A MANE Select	NP_002426.1:p.Asn273Lys
NM_001289155.2:c.819C>A	NP_001276084.1:p.Asn273Lys
NM_001289156.2:c.669C>A	NP_001276085.1:p.Asn223Lys
NM_001289157.2:c.636C>A	NP_001276086.1:p.Asn212Lys
NM_001330372.2:c.759C>A	NP_001317301.1:p.Asn253Lys