Canonical Allele Identifier: CA469813043

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926379T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166622T>G , CM000672.2:g.68166622T>G	GRCh38
NC_000010.10:g.69926379T>G , CM000672.1:g.69926379T>G	GRCh37
NC_000010.9:g.69596385T>G	NCBI36
NG_032118.1:g.65506T>G , LRG_410:g.65506T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1104T>G	ENSP00000346369.2:p.Ser368=
ENST00000373675.4:c.1929T>G	ENSP00000362779.4:p.Ser643=
ENST00000540630.6:c.1983T>G	ENSP00000441668.3:p.Ser661=
ENST00000613327.5:c.1929T>G	ENSP00000480757.2:p.Ser643=
ENST00000687572.1:c.807T>G	ENSP00000510427.1:p.Ser269=
ENST00000688812.1:c.1905T>G	ENSP00000510658.1:p.Ser635=
ENST00000690544.1:c.*1200T>G	ENSP00000508989.1:n.*1200T>G
ENST00000358913.10:c.1929T>G MANE Select	ENSP00000351790.5:p.Ser643=
ENST00000354393.6:c.1104T>G	ENSP00000346369.2:p.Ser368=
ENST00000358913.9:c.1929T>G	ENSP00000351790.5:p.Ser643=
ENST00000540630.5:c.1929T>G	ENSP00000441668.2:p.Ser643=
ENST00000613327.4:c.1047T>G	ENSP00000480757.1:p.Ser349=
NM_001256267.1:c.1929T>G	NP_001243196.1:p.Ser643=
NM_001256268.1:c.1047T>G	NP_001243197.1:p.Ser349=
NM_032578.3:c.1929T>G , LRG_410t1:c.1929T>G	NP_115967.2:p.Ser643=
NR_045662.3:n.1356T>G
NR_045663.3:n.2197T>G
XM_006718043.2:c.1983T>G	XP_006718106.1:p.Ser661=
XM_011540292.1:c.1959T>G	XP_011538594.1:p.Ser653=
XM_017016833.1:c.2007T>G	XP_016872322.1:p.Ser669=
XM_017016834.2:c.1929T>G	XP_016872323.1:p.Ser643=
XM_024448236.1:c.807T>G	XP_024304004.1:p.Ser269=
NR_045662.4:n.1466T>G
NR_045663.4:n.2142T>G
NM_001256267.2:c.1929T>G	NP_001243196.1:p.Ser643=
NM_001256268.2:c.1047T>G	NP_001243197.1:p.Ser349=
NM_032578.4:c.1929T>G MANE Select	NP_115967.2:p.Ser643=