Canonical Allele Identifier: CA376858891

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199379A>C , CM000672.2:g.68199379A>C	GRCh38
NC_000010.10:g.69959136A>C , CM000672.1:g.69959136A>C	GRCh37
NC_000010.9:g.69629142A>C	NCBI36
NG_032118.1:g.98263A>C , LRG_410:g.98263A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3297A>C MANE Select	NP_115967.2:p.Leu1099Phe
ENST00000358913.10:c.3297A>C MANE Select	ENSP00000351790.5:p.Leu1099Phe
NM_001256267.1:c.3297A>C	NP_001243196.1:p.Leu1099Phe
NM_001256267.2:c.3297A>C	NP_001243196.1:p.Leu1099Phe
NM_001256268.1:c.2415A>C	NP_001243197.1:p.Leu805Phe
NM_001256268.2:c.2415A>C	NP_001243197.1:p.Leu805Phe
NM_032578.3:c.3297A>C , LRG_410t1:c.3297A>C	NP_115967.2:p.Leu1099Phe
NR_045662.3:n.2724A>C
NR_045662.4:n.2834A>C
NR_045663.3:n.3426A>C
NR_045663.4:n.3371A>C
ENST00000354393.6:c.2472A>C	ENSP00000346369.2:p.Leu824Phe
ENST00000354393.7:c.2472A>C	ENSP00000346369.2:p.Leu824Phe
ENST00000358913.9:c.3297A>C	ENSP00000351790.5:p.Leu1099Phe
ENST00000540630.5:c.3297A>C	ENSP00000441668.2:p.Leu1099Phe
ENST00000540630.6:c.3351A>C	ENSP00000441668.3:p.Leu1117Phe
ENST00000613327.4:c.2415A>C	ENSP00000480757.1:p.Leu805Phe
ENST00000613327.5:c.3297A>C	ENSP00000480757.2:p.Leu1099Phe
ENST00000688812.1:c.*560A>C	ENSP00000510658.1:n.*560A>C
ENST00000690544.1:c.*2568A>C	ENSP00000508989.1:n.*2568A>C
XM_006718043.2:c.3351A>C	XP_006718106.1:p.Leu1117Phe
XM_011540292.1:c.3327A>C	XP_011538594.1:p.Leu1109Phe
XM_017016833.1:c.3375A>C	XP_016872322.1:p.Leu1125Phe
XM_017016834.2:c.3297A>C	XP_016872323.1:p.Leu1099Phe
XM_024448236.1:c.2175A>C	XP_024304004.1:p.Leu725Phe
XR_946029.1:n.1804-104T>G