Canonical Allele Identifier: CA469812554

Gene: MYPN

Linked Data

• COSMIC: COSM4544219 ; COSM4544220 ; COSM4544221
• MyVariant Identifiers: chr10:g.69961617G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68201860G>A , CM000672.2:g.68201860G>A	GRCh38
NC_000010.10:g.69961617G>A , CM000672.1:g.69961617G>A	GRCh37
NC_000010.9:g.69631623G>A	NCBI36
NG_032118.1:g.100744G>A , LRG_410:g.100744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2700G>A	ENSP00000346369.2:p.Leu900=
ENST00000540630.6:c.3579G>A	ENSP00000441668.3:p.Leu1193=
ENST00000613327.5:c.3525G>A	ENSP00000480757.2:p.Leu1175=
ENST00000688812.1:c.*788G>A	ENSP00000510658.1:n.*788G>A
ENST00000690544.1:c.*2796G>A	ENSP00000508989.1:n.*2796G>A
ENST00000358913.10:c.3525G>A MANE Select	ENSP00000351790.5:p.Leu1175=
ENST00000354393.6:c.2700G>A	ENSP00000346369.2:p.Leu900=
ENST00000358913.9:c.3525G>A	ENSP00000351790.5:p.Leu1175=
ENST00000540630.5:c.3525G>A	ENSP00000441668.2:p.Leu1175=
ENST00000613327.4:c.2643G>A	ENSP00000480757.1:p.Leu881=
NM_001256267.1:c.3525G>A	NP_001243196.1:p.Leu1175=
NM_001256268.1:c.2643G>A	NP_001243197.1:p.Leu881=
NM_032578.3:c.3525G>A , LRG_410t1:c.3525G>A	NP_115967.2:p.Leu1175=
NR_045662.3:n.2952G>A
NR_045663.3:n.3654G>A
XM_006718043.2:c.3579G>A	XP_006718106.1:p.Leu1193=
XM_011540292.1:c.3555G>A	XP_011538594.1:p.Leu1185=
XR_946029.1:n.1803+2171C>T
XM_017016833.1:c.3603G>A	XP_016872322.1:p.Leu1201=
XM_017016834.2:c.3525G>A	XP_016872323.1:p.Leu1175=
XM_024448236.1:c.2403G>A	XP_024304004.1:p.Leu801=
NR_045662.4:n.3062G>A
NR_045663.4:n.3599G>A
NM_001256267.2:c.3525G>A	NP_001243196.1:p.Leu1175=
NM_001256268.2:c.2643G>A	NP_001243197.1:p.Leu881=
NM_032578.4:c.3525G>A MANE Select	NP_115967.2:p.Leu1175=