Canonical Allele Identifier: CA1917232483

Gene: MYPN

Linked Data

• dbSNP Id: rs1267411567
• gnomAD v4: 10-68210500-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210500G>A , CM000672.2:g.68210500G>A	GRCh38
NC_000010.10:g.69970257G>A , CM000672.1:g.69970257G>A	GRCh37
NC_000010.9:g.69640263G>A	NCBI36
NG_032118.1:g.109384G>A , LRG_410:g.109384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*45G>A	ENSP00000346369.2:n.*45G>A
ENST00000540630.6:c.*45G>A	ENSP00000441668.3:n.*45G>A
ENST00000613327.5:c.*45G>A	ENSP00000480757.2:n.*45G>A
ENST00000688812.1:c.*1271G>A	ENSP00000510658.1:n.*1271G>A
ENST00000690544.1:c.*3279G>A	ENSP00000508989.1:n.*3279G>A
ENST00000358913.10:c.*45G>A MANE Select	ENSP00000351790.5:n.*45G>A
ENST00000354393.6:c.*45G>A	ENSP00000346369.2:n.*45G>A
ENST00000358913.9:c.*45G>A	ENSP00000351790.5:n.*45G>A
ENST00000540630.5:c.*45G>A	ENSP00000441668.2:n.*45G>A
ENST00000613327.4:c.*45G>A	ENSP00000480757.1:n.*45G>A
NM_001256267.1:c.*45G>A	NP_001243196.1:n.*45G>A
NM_001256268.1:c.*45G>A	NP_001243197.1:n.*45G>A
NM_032578.3:c.*45G>A , LRG_410t1:c.*45G>A	NP_115967.2:n.*45G>A
NR_045662.3:n.3435G>A
NR_045663.3:n.4137G>A
XM_006718043.2:c.*45G>A	XP_006718106.1:n.*45G>A
XM_011540292.1:c.*45G>A	XP_011538594.1:n.*45G>A
XR_946029.1:n.1574+4788C>T
XM_017016833.1:c.*45G>A	XP_016872322.1:n.*45G>A
XM_017016834.2:c.*45G>A	XP_016872323.1:n.*45G>A
XM_024448236.1:c.*45G>A	XP_024304004.1:n.*45G>A
NR_045662.4:n.3545G>A
NR_045663.4:n.4082G>A
NM_001256267.2:c.*45G>A	NP_001243196.1:n.*45G>A
NM_001256268.2:c.*45G>A	NP_001243197.1:n.*45G>A
NM_032578.4:c.*45G>A MANE Select	NP_115967.2:n.*45G>A