Canonical Allele Identifier: CA376859057

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199429A>C , CM000672.2:g.68199429A>C	GRCh38
NC_000010.10:g.69959186A>C , CM000672.1:g.69959186A>C	GRCh37
NC_000010.9:g.69629192A>C	NCBI36
NG_032118.1:g.98313A>C , LRG_410:g.98313A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3347A>C MANE Select	NP_115967.2:p.Asp1116Ala
ENST00000358913.10:c.3347A>C MANE Select	ENSP00000351790.5:p.Asp1116Ala
NM_001256267.1:c.3347A>C	NP_001243196.1:p.Asp1116Ala
NM_001256267.2:c.3347A>C	NP_001243196.1:p.Asp1116Ala
NM_001256268.1:c.2465A>C	NP_001243197.1:p.Asp822Ala
NM_001256268.2:c.2465A>C	NP_001243197.1:p.Asp822Ala
NM_032578.3:c.3347A>C , LRG_410t1:c.3347A>C	NP_115967.2:p.Asp1116Ala
NR_045662.3:n.2774A>C
NR_045662.4:n.2884A>C
NR_045663.3:n.3476A>C
NR_045663.4:n.3421A>C
ENST00000354393.6:c.2522A>C	ENSP00000346369.2:p.Asp841Ala
ENST00000354393.7:c.2522A>C	ENSP00000346369.2:p.Asp841Ala
ENST00000358913.9:c.3347A>C	ENSP00000351790.5:p.Asp1116Ala
ENST00000540630.5:c.3347A>C	ENSP00000441668.2:p.Asp1116Ala
ENST00000540630.6:c.3401A>C	ENSP00000441668.3:p.Asp1134Ala
ENST00000613327.4:c.2465A>C	ENSP00000480757.1:p.Asp822Ala
ENST00000613327.5:c.3347A>C	ENSP00000480757.2:p.Asp1116Ala
ENST00000688812.1:c.*610A>C	ENSP00000510658.1:n.*610A>C
ENST00000690544.1:c.*2618A>C	ENSP00000508989.1:n.*2618A>C
XM_006718043.2:c.3401A>C	XP_006718106.1:p.Asp1134Ala
XM_011540292.1:c.3377A>C	XP_011538594.1:p.Asp1126Ala
XM_017016833.1:c.3425A>C	XP_016872322.1:p.Asp1142Ala
XM_017016834.2:c.3347A>C	XP_016872323.1:p.Asp1116Ala
XM_024448236.1:c.2225A>C	XP_024304004.1:p.Asp742Ala
XR_946029.1:n.1804-154T>G