Canonical Allele Identifier: CA376859297

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199509A>C , CM000672.2:g.68199509A>C	GRCh38
NC_000010.10:g.69959266A>C , CM000672.1:g.69959266A>C	GRCh37
NC_000010.9:g.69629272A>C	NCBI36
NG_032118.1:g.98393A>C , LRG_410:g.98393A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3427A>C MANE Select	NP_115967.2:p.Thr1143Pro
ENST00000358913.10:c.3427A>C MANE Select	ENSP00000351790.5:p.Thr1143Pro
NM_001256267.1:c.3427A>C	NP_001243196.1:p.Thr1143Pro
NM_001256267.2:c.3427A>C	NP_001243196.1:p.Thr1143Pro
NM_001256268.1:c.2545A>C	NP_001243197.1:p.Thr849Pro
NM_001256268.2:c.2545A>C	NP_001243197.1:p.Thr849Pro
NM_032578.3:c.3427A>C , LRG_410t1:c.3427A>C	NP_115967.2:p.Thr1143Pro
NR_045662.3:n.2854A>C
NR_045662.4:n.2964A>C
NR_045663.3:n.3556A>C
NR_045663.4:n.3501A>C
ENST00000354393.6:c.2602A>C	ENSP00000346369.2:p.Thr868Pro
ENST00000354393.7:c.2602A>C	ENSP00000346369.2:p.Thr868Pro
ENST00000358913.9:c.3427A>C	ENSP00000351790.5:p.Thr1143Pro
ENST00000540630.5:c.3427A>C	ENSP00000441668.2:p.Thr1143Pro
ENST00000540630.6:c.3481A>C	ENSP00000441668.3:p.Thr1161Pro
ENST00000613327.4:c.2545A>C	ENSP00000480757.1:p.Thr849Pro
ENST00000613327.5:c.3427A>C	ENSP00000480757.2:p.Thr1143Pro
ENST00000688812.1:c.*690A>C	ENSP00000510658.1:n.*690A>C
ENST00000690544.1:c.*2698A>C	ENSP00000508989.1:n.*2698A>C
XM_006718043.2:c.3481A>C	XP_006718106.1:p.Thr1161Pro
XM_011540292.1:c.3457A>C	XP_011538594.1:p.Thr1153Pro
XM_017016833.1:c.3505A>C	XP_016872322.1:p.Thr1169Pro
XM_017016834.2:c.3427A>C	XP_016872323.1:p.Thr1143Pro
XM_024448236.1:c.2305A>C	XP_024304004.1:p.Thr769Pro
XR_946029.1:n.1804-234T>G