Canonical Allele Identifier: CA2609374273

Gene: MYPN

Linked Data

• gnomAD v4: 10-68210614-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210615dup , CM000672.2:g.68210615dup	GRCh38
NC_000010.10:g.69970372dup , CM000672.1:g.69970372dup	GRCh37
NC_000010.9:g.69640378dup	NCBI36
NG_032118.1:g.109499dup , LRG_410:g.109499dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*160dup	ENSP00000346369.2:n.*160dup
ENST00000540630.6:c.*160dup	ENSP00000441668.3:n.*160dup
ENST00000613327.5:c.*160dup	ENSP00000480757.2:n.*160dup
ENST00000688812.1:c.*1386dup	ENSP00000510658.1:n.*1386dup
ENST00000690544.1:c.*3394dup	ENSP00000508989.1:n.*3394dup
ENST00000358913.10:c.*160dup MANE Select	ENSP00000351790.5:n.*160dup
ENST00000354393.6:c.*160dup	ENSP00000346369.2:n.*160dup
ENST00000358913.9:c.*160dup	ENSP00000351790.5:n.*160dup
ENST00000540630.5:c.*160dup	ENSP00000441668.2:n.*160dup
ENST00000613327.4:c.*160dup	ENSP00000480757.1:n.*160dup
NM_001256267.1:c.*160dup	NP_001243196.1:n.*160dup
NM_001256268.1:c.*160dup	NP_001243197.1:n.*160dup
NM_032578.3:c.*160dup , LRG_410t1:c.*160dup	NP_115967.2:n.*160dup
NR_045662.3:n.3550dup
NR_045663.3:n.4252dup
XM_006718043.2:c.*160dup	XP_006718106.1:n.*160dup
XM_011540292.1:c.*160dup	XP_011538594.1:n.*160dup
XR_946029.1:n.1574+4673dup
XM_017016833.1:c.*160dup	XP_016872322.1:n.*160dup
XM_017016834.2:c.*160dup	XP_016872323.1:n.*160dup
XM_024448236.1:c.*160dup	XP_024304004.1:n.*160dup
NR_045662.4:n.3660dup
NR_045663.4:n.4197dup
NM_001256267.2:c.*160dup	NP_001243196.1:n.*160dup
NM_001256268.2:c.*160dup	NP_001243197.1:n.*160dup
NM_032578.4:c.*160dup MANE Select	NP_115967.2:n.*160dup