Canonical Allele Identifier: CA2609372307

Gene: MYPN

Linked Data

• gnomAD v4: 10-68165781-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165783del , CM000672.2:g.68165783del	GRCh38
NC_000010.10:g.69925540del , CM000672.1:g.69925540del	GRCh37
NC_000010.9:g.69595546del	NCBI36
NG_032118.1:g.64667del , LRG_410:g.64667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.740del	ENSP00000346369.2:p.Gly247AlafsTer11
ENST00000373675.4:c.1565del	ENSP00000362779.4:p.Gly522AlafsTer11
ENST00000540630.6:c.1619del	ENSP00000441668.3:p.Gly540AlafsTer11
ENST00000613327.5:c.1565del	ENSP00000480757.2:p.Gly522AlafsTer11
ENST00000687572.1:c.443del	ENSP00000510427.1:p.Gly148AlafsTer11
ENST00000687705.1:c.*1814del	ENSP00000509639.1:n.*1814del
ENST00000688812.1:c.1541del	ENSP00000510658.1:p.Gly514AlafsTer11
ENST00000689002.1:n.617del
ENST00000690544.1:c.*836del	ENSP00000508989.1:n.*836del
ENST00000358913.10:c.1565del MANE Select	ENSP00000351790.5:p.Gly522AlafsTer11
ENST00000354393.6:c.740del	ENSP00000346369.2:p.Gly247AlafsTer11
ENST00000358913.9:c.1565del	ENSP00000351790.5:p.Gly522AlafsTer11
ENST00000540630.5:c.1565del	ENSP00000441668.2:p.Gly522AlafsTer11
ENST00000613327.4:c.683del	ENSP00000480757.1:p.Gly228AlafsTer11
NM_001256267.1:c.1565del	NP_001243196.1:p.Gly522AlafsTer11
NM_001256268.1:c.683del	NP_001243197.1:p.Gly228AlafsTer11
NM_032578.3:c.1565del , LRG_410t1:c.1565del	NP_115967.2:p.Gly522AlafsTer11
NR_045662.3:n.992del
NR_045663.3:n.1833del
XM_006718043.2:c.1619del	XP_006718106.1:p.Gly540AlafsTer11
XM_011540292.1:c.1595del	XP_011538594.1:p.Gly532AlafsTer11
XM_017016833.1:c.1643del	XP_016872322.1:p.Gly548AlafsTer11
XM_017016834.2:c.1565del	XP_016872323.1:p.Gly522AlafsTer11
XM_024448236.1:c.443del	XP_024304004.1:p.Gly148AlafsTer11
NR_045662.4:n.1102del
NR_045663.4:n.1778del
NM_001256267.2:c.1565del	NP_001243196.1:p.Gly522AlafsTer11
NM_001256268.2:c.683del	NP_001243197.1:p.Gly228AlafsTer11
NM_032578.4:c.1565del MANE Select	NP_115967.2:p.Gly522AlafsTer11