Canonical Allele Identifier: CA1917227378

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199394G= , CM000672.2:g.68199394G=	GRCh38
NC_000010.10:g.69959151G= , CM000672.1:g.69959151G=	GRCh37
NC_000010.9:g.69629157G=	NCBI36
NG_032118.1:g.98278G= , LRG_410:g.98278G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2487G=	ENSP00000346369.2:p.Leu829=
ENST00000540630.6:c.3366G=	ENSP00000441668.3:p.Leu1122=
ENST00000613327.5:c.3312G=	ENSP00000480757.2:p.Leu1104=
ENST00000688812.1:c.*575G=	ENSP00000510658.1:n.*575G=
ENST00000690544.1:c.*2583G=	ENSP00000508989.1:n.*2583G=
ENST00000358913.10:c.3312G= MANE Select	ENSP00000351790.5:p.Leu1104=
ENST00000354393.6:c.2487G=	ENSP00000346369.2:p.Leu829=
ENST00000358913.9:c.3312G=	ENSP00000351790.5:p.Leu1104=
ENST00000540630.5:c.3312G=	ENSP00000441668.2:p.Leu1104=
ENST00000613327.4:c.2430G=	ENSP00000480757.1:p.Leu810=
NM_001256267.1:c.3312G=	NP_001243196.1:p.Leu1104=
NM_001256268.1:c.2430G=	NP_001243197.1:p.Leu810=
NM_032578.3:c.3312G= , LRG_410t1:c.3312G=	NP_115967.2:p.Leu1104=
NR_045662.3:n.2739G=
NR_045663.3:n.3441G=
XM_006718043.2:c.3366G=	XP_006718106.1:p.Leu1122=
XM_011540292.1:c.3342G=	XP_011538594.1:p.Leu1114=
XR_946029.1:n.1804-119C=
XM_017016833.1:c.3390G=	XP_016872322.1:p.Leu1130=
XM_017016834.2:c.3312G=	XP_016872323.1:p.Leu1104=
XM_024448236.1:c.2190G=	XP_024304004.1:p.Leu730=
NR_045662.4:n.2849G=
NR_045663.4:n.3386G=
NM_001256267.2:c.3312G=	NP_001243196.1:p.Leu1104=
NM_001256268.2:c.2430G=	NP_001243197.1:p.Leu810=
NM_032578.4:c.3312G= MANE Select	NP_115967.2:p.Leu1104=