Canonical Allele Identifier: CA376859252

Gene: MYPN

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199486C>A , CM000672.2:g.68199486C>A	GRCh38
NC_000010.10:g.69959243C>A , CM000672.1:g.69959243C>A	GRCh37
NC_000010.9:g.69629249C>A	NCBI36
NG_032118.1:g.98370C>A , LRG_410:g.98370C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2579C>A	ENSP00000346369.2:p.Pro860Gln
ENST00000540630.6:c.3458C>A	ENSP00000441668.3:p.Pro1153Gln
ENST00000613327.5:c.3404C>A	ENSP00000480757.2:p.Pro1135Gln
ENST00000688812.1:c.*667C>A	ENSP00000510658.1:n.*667C>A
ENST00000690544.1:c.*2675C>A	ENSP00000508989.1:n.*2675C>A
ENST00000358913.10:c.3404C>A MANE Select	ENSP00000351790.5:p.Pro1135Gln
ENST00000354393.6:c.2579C>A	ENSP00000346369.2:p.Pro860Gln
ENST00000358913.9:c.3404C>A	ENSP00000351790.5:p.Pro1135Gln
ENST00000540630.5:c.3404C>A	ENSP00000441668.2:p.Pro1135Gln
ENST00000613327.4:c.2522C>A	ENSP00000480757.1:p.Pro841Gln
NM_001256267.1:c.3404C>A	NP_001243196.1:p.Pro1135Gln
NM_001256268.1:c.2522C>A	NP_001243197.1:p.Pro841Gln
NM_032578.3:c.3404C>A , LRG_410t1:c.3404C>A	NP_115967.2:p.Pro1135Gln
NR_045662.3:n.2831C>A
NR_045663.3:n.3533C>A
XM_006718043.2:c.3458C>A	XP_006718106.1:p.Pro1153Gln
XM_011540292.1:c.3434C>A	XP_011538594.1:p.Pro1145Gln
XR_946029.1:n.1804-211G>T
XM_017016833.1:c.3482C>A	XP_016872322.1:p.Pro1161Gln
XM_017016834.2:c.3404C>A	XP_016872323.1:p.Pro1135Gln
XM_024448236.1:c.2282C>A	XP_024304004.1:p.Pro761Gln
NR_045662.4:n.2941C>A
NR_045663.4:n.3478C>A
NM_001256267.2:c.3404C>A	NP_001243196.1:p.Pro1135Gln
NM_001256268.2:c.2522C>A	NP_001243197.1:p.Pro841Gln
NM_032578.4:c.3404C>A MANE Select	NP_115967.2:p.Pro1135Gln