Canonical Allele Identifier: CA469812442

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959220A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199463A>G , CM000672.2:g.68199463A>G	GRCh38
NC_000010.10:g.69959220A>G , CM000672.1:g.69959220A>G	GRCh37
NC_000010.9:g.69629226A>G	NCBI36
NG_032118.1:g.98347A>G , LRG_410:g.98347A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2556A>G	ENSP00000346369.2:p.Gly852=
ENST00000540630.6:c.3435A>G	ENSP00000441668.3:p.Gly1145=
ENST00000613327.5:c.3381A>G	ENSP00000480757.2:p.Gly1127=
ENST00000688812.1:c.*644A>G	ENSP00000510658.1:n.*644A>G
ENST00000690544.1:c.*2652A>G	ENSP00000508989.1:n.*2652A>G
ENST00000358913.10:c.3381A>G MANE Select	ENSP00000351790.5:p.Gly1127=
ENST00000354393.6:c.2556A>G	ENSP00000346369.2:p.Gly852=
ENST00000358913.9:c.3381A>G	ENSP00000351790.5:p.Gly1127=
ENST00000540630.5:c.3381A>G	ENSP00000441668.2:p.Gly1127=
ENST00000613327.4:c.2499A>G	ENSP00000480757.1:p.Gly833=
NM_001256267.1:c.3381A>G	NP_001243196.1:p.Gly1127=
NM_001256268.1:c.2499A>G	NP_001243197.1:p.Gly833=
NM_032578.3:c.3381A>G , LRG_410t1:c.3381A>G	NP_115967.2:p.Gly1127=
NR_045662.3:n.2808A>G
NR_045663.3:n.3510A>G
XM_006718043.2:c.3435A>G	XP_006718106.1:p.Gly1145=
XM_011540292.1:c.3411A>G	XP_011538594.1:p.Gly1137=
XR_946029.1:n.1804-188T>C
XM_017016833.1:c.3459A>G	XP_016872322.1:p.Gly1153=
XM_017016834.2:c.3381A>G	XP_016872323.1:p.Gly1127=
XM_024448236.1:c.2259A>G	XP_024304004.1:p.Gly753=
NR_045662.4:n.2918A>G
NR_045663.4:n.3455A>G
NM_001256267.2:c.3381A>G	NP_001243196.1:p.Gly1127=
NM_001256268.2:c.2499A>G	NP_001243197.1:p.Gly833=
NM_032578.4:c.3381A>G MANE Select	NP_115967.2:p.Gly1127=