Canonical Allele Identifier: CA2609372497

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166530-TCCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166531_68166533del , CM000672.2:g.68166531_68166533del	GRCh38
NC_000010.10:g.69926288_69926290del , CM000672.1:g.69926288_69926290del	GRCh37
NC_000010.9:g.69596294_69596296del	NCBI36
NG_032118.1:g.65415_65417del , LRG_410:g.65415_65417del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1013_1015del	ENSP00000346369.2:p.Ser338Ter
ENST00000373675.4:c.1838_1840del	ENSP00000362779.4:p.Ser613Ter
ENST00000540630.6:c.1892_1894del	ENSP00000441668.3:p.Ser631Ter
ENST00000613327.5:c.1838_1840del	ENSP00000480757.2:p.Ser613Ter
ENST00000687572.1:c.716_718del	ENSP00000510427.1:p.Ser239Ter
ENST00000688812.1:c.1814_1816del	ENSP00000510658.1:p.Ser605Ter
ENST00000690544.1:c.*1109_*1111del	ENSP00000508989.1:n.*1109_*1111del
ENST00000358913.10:c.1838_1840del MANE Select	ENSP00000351790.5:p.Ser613Ter
ENST00000354393.6:c.1013_1015del	ENSP00000346369.2:p.Ser338Ter
ENST00000358913.9:c.1838_1840del	ENSP00000351790.5:p.Ser613Ter
ENST00000540630.5:c.1838_1840del	ENSP00000441668.2:p.Ser613Ter
ENST00000613327.4:c.956_958del	ENSP00000480757.1:p.Ser319Ter
NM_001256267.1:c.1838_1840del	NP_001243196.1:p.Ser613Ter
NM_001256268.1:c.956_958del	NP_001243197.1:p.Ser319Ter
NM_032578.3:c.1838_1840del , LRG_410t1:c.1838_1840del	NP_115967.2:p.Ser613Ter
NR_045662.3:n.1265_1267del
NR_045663.3:n.2106_2108del
XM_006718043.2:c.1892_1894del	XP_006718106.1:p.Ser631Ter
XM_011540292.1:c.1868_1870del	XP_011538594.1:p.Ser623Ter
XM_017016833.1:c.1916_1918del	XP_016872322.1:p.Ser639Ter
XM_017016834.2:c.1838_1840del	XP_016872323.1:p.Ser613Ter
XM_024448236.1:c.716_718del	XP_024304004.1:p.Ser239Ter
NR_045662.4:n.1375_1377del
NR_045663.4:n.2051_2053del
NM_001256267.2:c.1838_1840del	NP_001243196.1:p.Ser613Ter
NM_001256268.2:c.956_958del	NP_001243197.1:p.Ser319Ter
NM_032578.4:c.1838_1840del MANE Select	NP_115967.2:p.Ser613Ter