Canonical Allele Identifier: CA2609374282

Gene: MYPN

Linked Data

• gnomAD v4: 10-68210629-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210629A>G , CM000672.2:g.68210629A>G	GRCh38
NC_000010.10:g.69970386A>G , CM000672.1:g.69970386A>G	GRCh37
NC_000010.9:g.69640392A>G	NCBI36
NG_032118.1:g.109513A>G , LRG_410:g.109513A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*174A>G	ENSP00000346369.2:n.*174A>G
ENST00000540630.6:c.*174A>G	ENSP00000441668.3:n.*174A>G
ENST00000613327.5:c.*174A>G	ENSP00000480757.2:n.*174A>G
ENST00000688812.1:c.*1400A>G	ENSP00000510658.1:n.*1400A>G
ENST00000690544.1:c.*3408A>G	ENSP00000508989.1:n.*3408A>G
ENST00000358913.10:c.*174A>G MANE Select	ENSP00000351790.5:n.*174A>G
ENST00000354393.6:c.*174A>G	ENSP00000346369.2:n.*174A>G
ENST00000358913.9:c.*174A>G	ENSP00000351790.5:n.*174A>G
ENST00000540630.5:c.*174A>G	ENSP00000441668.2:n.*174A>G
ENST00000613327.4:c.*174A>G	ENSP00000480757.1:n.*174A>G
NM_001256267.1:c.*174A>G	NP_001243196.1:n.*174A>G
NM_001256268.1:c.*174A>G	NP_001243197.1:n.*174A>G
NM_032578.3:c.*174A>G , LRG_410t1:c.*174A>G	NP_115967.2:n.*174A>G
NR_045662.3:n.3564A>G
NR_045663.3:n.4266A>G
XM_006718043.2:c.*174A>G	XP_006718106.1:n.*174A>G
XM_011540292.1:c.*174A>G	XP_011538594.1:n.*174A>G
XR_946029.1:n.1574+4659T>C
XM_017016833.1:c.*174A>G	XP_016872322.1:n.*174A>G
XM_017016834.2:c.*174A>G	XP_016872323.1:n.*174A>G
XM_024448236.1:c.*174A>G	XP_024304004.1:n.*174A>G
NR_045662.4:n.3674A>G
NR_045663.4:n.4211A>G
NM_001256267.2:c.*174A>G	NP_001243196.1:n.*174A>G
NM_001256268.2:c.*174A>G	NP_001243197.1:n.*174A>G
NM_032578.4:c.*174A>G MANE Select	NP_115967.2:n.*174A>G