Canonical Allele Identifier: CA5522472

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68148422A>G , CM000672.2:g.68148422A>G	GRCh38
NC_000010.10:g.69908179A>G , CM000672.1:g.69908179A>G	GRCh37
NC_000010.9:g.69578185A>G	NCBI36
NG_032118.1:g.47306A>G , LRG_410:g.47306A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.1200A>G MANE Select	NP_115967.2:p.Gln400=
ENST00000358913.10:c.1200A>G MANE Select	ENSP00000351790.5:p.Gln400=
NM_001256267.1:c.1200A>G	NP_001243196.1:p.Gln400=
NM_001256267.2:c.1200A>G	NP_001243196.1:p.Gln400=
NM_001256268.1:c.318A>G	NP_001243197.1:p.Gln106=
NM_001256268.2:c.318A>G	NP_001243197.1:p.Gln106=
NM_032578.3:c.1200A>G , LRG_410t1:c.1200A>G	NP_115967.2:p.Gln400=
NR_045662.3:n.627A>G
NR_045662.4:n.737A>G
NR_045663.3:n.1492A>G
NR_045663.4:n.1437A>G
ENST00000354393.6:c.375A>G	ENSP00000346369.2:p.Gln125=
ENST00000354393.7:c.375A>G	ENSP00000346369.2:p.Gln125=
ENST00000358913.9:c.1200A>G	ENSP00000351790.5:p.Gln400=
ENST00000373675.3:c.1200A>G	ENSP00000362779.3:p.Gln400=
ENST00000373675.4:c.1200A>G	ENSP00000362779.4:p.Gln400=
ENST00000540630.5:c.1200A>G	ENSP00000441668.2:p.Gln400=
ENST00000540630.6:c.1254A>G	ENSP00000441668.3:p.Gln418=
ENST00000613327.4:c.318A>G	ENSP00000480757.1:p.Gln106=
ENST00000613327.5:c.1200A>G	ENSP00000480757.2:p.Gln400=
ENST00000685006.1:c.1272A>G	ENSP00000510318.1:p.Gln424=
ENST00000685060.1:n.1437A>G
ENST00000685154.1:c.1200A>G	ENSP00000509251.1:p.Gln400=
ENST00000686289.1:n.411A>G
ENST00000687572.1:c.78A>G	ENSP00000510427.1:p.Gln26=
ENST00000687705.1:c.*1449A>G	ENSP00000509639.1:n.*1449A>G
ENST00000688812.1:c.1200A>G	ENSP00000510658.1:p.Gln400=
ENST00000689218.1:n.1429A>G
ENST00000689484.1:c.78A>G	ENSP00000509884.1:p.Gln26=
ENST00000689797.1:c.78A>G	ENSP00000510689.1:p.Gln26=
ENST00000690544.1:c.*471A>G	ENSP00000508989.1:n.*471A>G
ENST00000692953.1:n.360A>G
ENST00000692979.1:c.1200A>G	ENSP00000509849.1:p.Gln400=
ENST00000693699.1:c.229-1618A>G
XM_006718043.2:c.1254A>G	XP_006718106.1:p.Gln418=
XM_011540292.1:c.1254A>G	XP_011538594.1:p.Gln418=
XM_017016833.1:c.1278A>G	XP_016872322.1:p.Gln426=
XM_017016834.2:c.1200A>G	XP_016872323.1:p.Gln400=
XM_024448236.1:c.78A>G	XP_024304004.1:p.Gln26=
XR_001747479.1:n.455-1704T>C