Canonical Allele Identifier: CA2609374264

Gene: MYPN

Linked Data

• gnomAD v4: 10-68210602-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210602A>G , CM000672.2:g.68210602A>G	GRCh38
NC_000010.10:g.69970359A>G , CM000672.1:g.69970359A>G	GRCh37
NC_000010.9:g.69640365A>G	NCBI36
NG_032118.1:g.109486A>G , LRG_410:g.109486A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*147A>G	ENSP00000346369.2:n.*147A>G
ENST00000540630.6:c.*147A>G	ENSP00000441668.3:n.*147A>G
ENST00000613327.5:c.*147A>G	ENSP00000480757.2:n.*147A>G
ENST00000688812.1:c.*1373A>G	ENSP00000510658.1:n.*1373A>G
ENST00000690544.1:c.*3381A>G	ENSP00000508989.1:n.*3381A>G
ENST00000358913.10:c.*147A>G MANE Select	ENSP00000351790.5:n.*147A>G
ENST00000354393.6:c.*147A>G	ENSP00000346369.2:n.*147A>G
ENST00000358913.9:c.*147A>G	ENSP00000351790.5:n.*147A>G
ENST00000540630.5:c.*147A>G	ENSP00000441668.2:n.*147A>G
ENST00000613327.4:c.*147A>G	ENSP00000480757.1:n.*147A>G
NM_001256267.1:c.*147A>G	NP_001243196.1:n.*147A>G
NM_001256268.1:c.*147A>G	NP_001243197.1:n.*147A>G
NM_032578.3:c.*147A>G , LRG_410t1:c.*147A>G	NP_115967.2:n.*147A>G
NR_045662.3:n.3537A>G
NR_045663.3:n.4239A>G
XM_006718043.2:c.*147A>G	XP_006718106.1:n.*147A>G
XM_011540292.1:c.*147A>G	XP_011538594.1:n.*147A>G
XR_946029.1:n.1574+4686T>C
XM_017016833.1:c.*147A>G	XP_016872322.1:n.*147A>G
XM_017016834.2:c.*147A>G	XP_016872323.1:n.*147A>G
XM_024448236.1:c.*147A>G	XP_024304004.1:n.*147A>G
NR_045662.4:n.3647A>G
NR_045663.4:n.4184A>G
NM_001256267.2:c.*147A>G	NP_001243196.1:n.*147A>G
NM_001256268.2:c.*147A>G	NP_001243197.1:n.*147A>G
NM_032578.4:c.*147A>G MANE Select	NP_115967.2:n.*147A>G