Canonical Allele Identifier: CA1917227437

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199521A= , CM000672.2:g.68199521A=	GRCh38
NC_000010.10:g.69959278A= , CM000672.1:g.69959278A=	GRCh37
NC_000010.9:g.69629284A=	NCBI36
NG_032118.1:g.98405A= , LRG_410:g.98405A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3439A= MANE Select	NP_115967.2:p.Ile1147=
ENST00000358913.10:c.3439A= MANE Select	ENSP00000351790.5:p.Ile1147=
NM_001256267.1:c.3439A=	NP_001243196.1:p.Ile1147=
NM_001256267.2:c.3439A=	NP_001243196.1:p.Ile1147=
NM_001256268.1:c.2557A=	NP_001243197.1:p.Ile853=
NM_001256268.2:c.2557A=	NP_001243197.1:p.Ile853=
NM_032578.3:c.3439A= , LRG_410t1:c.3439A=	NP_115967.2:p.Ile1147=
NR_045662.3:n.2866A=
NR_045662.4:n.2976A=
NR_045663.3:n.3568A=
NR_045663.4:n.3513A=
ENST00000354393.6:c.2614A=	ENSP00000346369.2:p.Ile872=
ENST00000354393.7:c.2614A=	ENSP00000346369.2:p.Ile872=
ENST00000358913.9:c.3439A=	ENSP00000351790.5:p.Ile1147=
ENST00000540630.5:c.3439A=	ENSP00000441668.2:p.Ile1147=
ENST00000540630.6:c.3493A=	ENSP00000441668.3:p.Ile1165=
ENST00000613327.4:c.2557A=	ENSP00000480757.1:p.Ile853=
ENST00000613327.5:c.3439A=	ENSP00000480757.2:p.Ile1147=
ENST00000688812.1:c.*702A=	ENSP00000510658.1:n.*702A=
ENST00000690544.1:c.*2710A=	ENSP00000508989.1:n.*2710A=
XM_006718043.2:c.3493A=	XP_006718106.1:p.Ile1165=
XM_011540292.1:c.3469A=	XP_011538594.1:p.Ile1157=
XM_017016833.1:c.3517A=	XP_016872322.1:p.Ile1173=
XM_017016834.2:c.3439A=	XP_016872323.1:p.Ile1147=
XM_024448236.1:c.2317A=	XP_024304004.1:p.Ile773=
XR_946029.1:n.1804-246T=