Canonical Allele Identifier: CA1917215970

Gene: MYPN

Linked Data

• dbSNP Id: rs2043061824
• gnomAD v4: 10-68166724-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166727_68166729del , CM000672.2:g.68166727_68166729del	GRCh38
NC_000010.10:g.69926484_69926486del , CM000672.1:g.69926484_69926486del	GRCh37
NC_000010.9:g.69596490_69596492del	NCBI36
NG_032118.1:g.65611_65613del , LRG_410:g.65611_65613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1148+61_1148+63del	ENSP00000346369.2:n.1148+61_1148+63del
ENST00000540630.6:c.2027+61_2027+63del	ENSP00000441668.3:n.2027+61_2027+63del
ENST00000613327.5:c.1973+61_1973+63del	ENSP00000480757.2:n.1973+61_1973+63del
ENST00000688812.1:c.1949+61_1949+63del	ENSP00000510658.1:n.1949+61_1949+63del
ENST00000690544.1:c.*1244+61_*1244+63del	ENSP00000508989.1:n.*1244+61_*1244+63del
ENST00000358913.10:c.1973+61_1973+63del MANE Select	ENSP00000351790.5:n.1973+61_1973+63del
ENST00000354393.6:c.1148+61_1148+63del	ENSP00000346369.2:n.1148+61_1148+63del
ENST00000358913.9:c.1973+61_1973+63del	ENSP00000351790.5:n.1973+61_1973+63del
ENST00000540630.5:c.1973+61_1973+63del	ENSP00000441668.2:n.1973+61_1973+63del
ENST00000613327.4:c.1091+61_1091+63del	ENSP00000480757.1:n.1091+61_1091+63del
NM_001256267.1:c.1973+61_1973+63del	NP_001243196.1:n.1973+61_1973+63del
NM_001256268.1:c.1091+61_1091+63del	NP_001243197.1:n.1091+61_1091+63del
NM_032578.3:c.1973+61_1973+63del , LRG_410t1:c.1973+61_1973+63del	NP_115967.2:n.1973+61_1973+63del
NR_045662.3:n.1400+61_1400+63del
NR_045663.3:n.2241+61_2241+63del
XM_006718043.2:c.2027+61_2027+63del	XP_006718106.1:n.2027+61_2027+63del
XM_011540292.1:c.2003+61_2003+63del	XP_011538594.1:n.2003+61_2003+63del
XM_017016833.1:c.2051+61_2051+63del	XP_016872322.1:n.2051+61_2051+63del
XM_017016834.2:c.1973+61_1973+63del	XP_016872323.1:n.1973+61_1973+63del
XM_024448236.1:c.851+61_851+63del	XP_024304004.1:n.851+61_851+63del
NR_045662.4:n.1510+61_1510+63del
NR_045663.4:n.2186+61_2186+63del
NM_001256267.2:c.1973+61_1973+63del	NP_001243196.1:n.1973+61_1973+63del
NM_001256268.2:c.1091+61_1091+63del	NP_001243197.1:n.1091+61_1091+63del
NM_032578.4:c.1973+61_1973+63del MANE Select	NP_115967.2:n.1973+61_1973+63del