Canonical Allele Identifier: CA469812449

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959226C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199469C>T , CM000672.2:g.68199469C>T	GRCh38
NC_000010.10:g.69959226C>T , CM000672.1:g.69959226C>T	GRCh37
NC_000010.9:g.69629232C>T	NCBI36
NG_032118.1:g.98353C>T , LRG_410:g.98353C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2562C>T	ENSP00000346369.2:p.His854=
ENST00000540630.6:c.3441C>T	ENSP00000441668.3:p.His1147=
ENST00000613327.5:c.3387C>T	ENSP00000480757.2:p.His1129=
ENST00000688812.1:c.*650C>T	ENSP00000510658.1:n.*650C>T
ENST00000690544.1:c.*2658C>T	ENSP00000508989.1:n.*2658C>T
ENST00000358913.10:c.3387C>T MANE Select	ENSP00000351790.5:p.His1129=
ENST00000354393.6:c.2562C>T	ENSP00000346369.2:p.His854=
ENST00000358913.9:c.3387C>T	ENSP00000351790.5:p.His1129=
ENST00000540630.5:c.3387C>T	ENSP00000441668.2:p.His1129=
ENST00000613327.4:c.2505C>T	ENSP00000480757.1:p.His835=
NM_001256267.1:c.3387C>T	NP_001243196.1:p.His1129=
NM_001256268.1:c.2505C>T	NP_001243197.1:p.His835=
NM_032578.3:c.3387C>T , LRG_410t1:c.3387C>T	NP_115967.2:p.His1129=
NR_045662.3:n.2814C>T
NR_045663.3:n.3516C>T
XM_006718043.2:c.3441C>T	XP_006718106.1:p.His1147=
XM_011540292.1:c.3417C>T	XP_011538594.1:p.His1139=
XR_946029.1:n.1804-194G>A
XM_017016833.1:c.3465C>T	XP_016872322.1:p.His1155=
XM_017016834.2:c.3387C>T	XP_016872323.1:p.His1129=
XM_024448236.1:c.2265C>T	XP_024304004.1:p.His755=
NR_045662.4:n.2924C>T
NR_045663.4:n.3461C>T
NM_001256267.2:c.3387C>T	NP_001243196.1:p.His1129=
NM_001256268.2:c.2505C>T	NP_001243197.1:p.His835=
NM_032578.4:c.3387C>T MANE Select	NP_115967.2:p.His1129=