Canonical Allele Identifier: CA1917227433

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199513A= , CM000672.2:g.68199513A=	GRCh38
NC_000010.10:g.69959270A= , CM000672.1:g.69959270A=	GRCh37
NC_000010.9:g.69629276A=	NCBI36
NG_032118.1:g.98397A= , LRG_410:g.98397A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3431A= MANE Select	NP_115967.2:p.Tyr1144=
ENST00000358913.10:c.3431A= MANE Select	ENSP00000351790.5:p.Tyr1144=
NM_001256267.1:c.3431A=	NP_001243196.1:p.Tyr1144=
NM_001256267.2:c.3431A=	NP_001243196.1:p.Tyr1144=
NM_001256268.1:c.2549A=	NP_001243197.1:p.Tyr850=
NM_001256268.2:c.2549A=	NP_001243197.1:p.Tyr850=
NM_032578.3:c.3431A= , LRG_410t1:c.3431A=	NP_115967.2:p.Tyr1144=
NR_045662.3:n.2858A=
NR_045662.4:n.2968A=
NR_045663.3:n.3560A=
NR_045663.4:n.3505A=
ENST00000354393.6:c.2606A=	ENSP00000346369.2:p.Tyr869=
ENST00000354393.7:c.2606A=	ENSP00000346369.2:p.Tyr869=
ENST00000358913.9:c.3431A=	ENSP00000351790.5:p.Tyr1144=
ENST00000540630.5:c.3431A=	ENSP00000441668.2:p.Tyr1144=
ENST00000540630.6:c.3485A=	ENSP00000441668.3:p.Tyr1162=
ENST00000613327.4:c.2549A=	ENSP00000480757.1:p.Tyr850=
ENST00000613327.5:c.3431A=	ENSP00000480757.2:p.Tyr1144=
ENST00000688812.1:c.*694A=	ENSP00000510658.1:n.*694A=
ENST00000690544.1:c.*2702A=	ENSP00000508989.1:n.*2702A=
XM_006718043.2:c.3485A=	XP_006718106.1:p.Tyr1162=
XM_011540292.1:c.3461A=	XP_011538594.1:p.Tyr1154=
XM_017016833.1:c.3509A=	XP_016872322.1:p.Tyr1170=
XM_017016834.2:c.3431A=	XP_016872323.1:p.Tyr1144=
XM_024448236.1:c.2309A=	XP_024304004.1:p.Tyr770=
XR_946029.1:n.1804-238T=