Canonical Allele Identifier: CA376858963

Gene: MYPN

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199400G>A , CM000672.2:g.68199400G>A	GRCh38
NC_000010.10:g.69959157G>A , CM000672.1:g.69959157G>A	GRCh37
NC_000010.9:g.69629163G>A	NCBI36
NG_032118.1:g.98284G>A , LRG_410:g.98284G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2493G>A	ENSP00000346369.2:p.Trp831Ter
ENST00000540630.6:c.3372G>A	ENSP00000441668.3:p.Trp1124Ter
ENST00000613327.5:c.3318G>A	ENSP00000480757.2:p.Trp1106Ter
ENST00000688812.1:c.*581G>A	ENSP00000510658.1:n.*581G>A
ENST00000690544.1:c.*2589G>A	ENSP00000508989.1:n.*2589G>A
ENST00000358913.10:c.3318G>A MANE Select	ENSP00000351790.5:p.Trp1106Ter
ENST00000354393.6:c.2493G>A	ENSP00000346369.2:p.Trp831Ter
ENST00000358913.9:c.3318G>A	ENSP00000351790.5:p.Trp1106Ter
ENST00000540630.5:c.3318G>A	ENSP00000441668.2:p.Trp1106Ter
ENST00000613327.4:c.2436G>A	ENSP00000480757.1:p.Trp812Ter
NM_001256267.1:c.3318G>A	NP_001243196.1:p.Trp1106Ter
NM_001256268.1:c.2436G>A	NP_001243197.1:p.Trp812Ter
NM_032578.3:c.3318G>A , LRG_410t1:c.3318G>A	NP_115967.2:p.Trp1106Ter
NR_045662.3:n.2745G>A
NR_045663.3:n.3447G>A
XM_006718043.2:c.3372G>A	XP_006718106.1:p.Trp1124Ter
XM_011540292.1:c.3348G>A	XP_011538594.1:p.Trp1116Ter
XR_946029.1:n.1804-125C>T
XM_017016833.1:c.3396G>A	XP_016872322.1:p.Trp1132Ter
XM_017016834.2:c.3318G>A	XP_016872323.1:p.Trp1106Ter
XM_024448236.1:c.2196G>A	XP_024304004.1:p.Trp732Ter
NR_045662.4:n.2855G>A
NR_045663.4:n.3392G>A
NM_001256267.2:c.3318G>A	NP_001243196.1:p.Trp1106Ter
NM_001256268.2:c.2436G>A	NP_001243197.1:p.Trp812Ter
NM_032578.4:c.3318G>A MANE Select	NP_115967.2:p.Trp1106Ter