Canonical Allele Identifier: CA376857375

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955230C>A (hg19) ; chr10:g.68195473C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195473C>A , CM000672.2:g.68195473C>A	GRCh38
NC_000010.10:g.69955230C>A , CM000672.1:g.69955230C>A	GRCh37
NC_000010.9:g.69625236C>A	NCBI36
NG_032118.1:g.94357C>A , LRG_410:g.94357C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2274C>A	ENSP00000346369.2:p.His758Gln
ENST00000540630.6:c.3153C>A	ENSP00000441668.3:p.His1051Gln
ENST00000613327.5:c.3099C>A	ENSP00000480757.2:p.His1033Gln
ENST00000688812.1:c.*362C>A	ENSP00000510658.1:n.*362C>A
ENST00000690544.1:c.*2370C>A	ENSP00000508989.1:n.*2370C>A
ENST00000358913.10:c.3099C>A MANE Select	ENSP00000351790.5:p.His1033Gln
ENST00000354393.6:c.2274C>A	ENSP00000346369.2:p.His758Gln
ENST00000358913.9:c.3099C>A	ENSP00000351790.5:p.His1033Gln
ENST00000540630.5:c.3099C>A	ENSP00000441668.2:p.His1033Gln
ENST00000613327.4:c.2217C>A	ENSP00000480757.1:p.His739Gln
NM_001256267.1:c.3099C>A	NP_001243196.1:p.His1033Gln
NM_001256268.1:c.2217C>A	NP_001243197.1:p.His739Gln
NM_032578.3:c.3099C>A , LRG_410t1:c.3099C>A	NP_115967.2:p.His1033Gln
NR_045662.3:n.2526C>A
NR_045663.3:n.3228C>A
XM_006718043.2:c.3153C>A	XP_006718106.1:p.His1051Gln
XM_011540292.1:c.3129C>A	XP_011538594.1:p.His1043Gln
XM_017016833.1:c.3177C>A	XP_016872322.1:p.His1059Gln
XM_017016834.2:c.3099C>A	XP_016872323.1:p.His1033Gln
XM_024448236.1:c.1977C>A	XP_024304004.1:p.His659Gln
NR_045662.4:n.2636C>A
NR_045663.4:n.3173C>A
NM_001256267.2:c.3099C>A	NP_001243196.1:p.His1033Gln
NM_001256268.2:c.2217C>A	NP_001243197.1:p.His739Gln
NM_032578.4:c.3099C>A MANE Select	NP_115967.2:p.His1033Gln