Canonical Allele Identifier: CA376858882
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199377T>A , CM000672.2:g.68199377T>A GRCh38
NC_000010.10:g.69959134T>A , CM000672.1:g.69959134T>A GRCh37
NC_000010.9:g.69629140T>A NCBI36
NG_032118.1:g.98261T>A , LRG_410:g.98261T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2470T>A ENSP00000346369.2:p.Leu824Ile
ENST00000540630.6:c.3349T>A ENSP00000441668.3:p.Leu1117Ile
ENST00000613327.5:c.3295T>A ENSP00000480757.2:p.Leu1099Ile
ENST00000688812.1:c.*558T>A ENSP00000510658.1:n.*558T>A
ENST00000690544.1:c.*2566T>A ENSP00000508989.1:n.*2566T>A
ENST00000358913.10:c.3295T>A MANE Select ENSP00000351790.5:p.Leu1099Ile
ENST00000354393.6:c.2470T>A ENSP00000346369.2:p.Leu824Ile
ENST00000358913.9:c.3295T>A ENSP00000351790.5:p.Leu1099Ile
ENST00000540630.5:c.3295T>A ENSP00000441668.2:p.Leu1099Ile
ENST00000613327.4:c.2413T>A ENSP00000480757.1:p.Leu805Ile
NM_001256267.1:c.3295T>A NP_001243196.1:p.Leu1099Ile
NM_001256268.1:c.2413T>A NP_001243197.1:p.Leu805Ile
NM_032578.3:c.3295T>A , LRG_410t1:c.3295T>A NP_115967.2:p.Leu1099Ile
NR_045662.3:n.2722T>A
NR_045663.3:n.3424T>A
XM_006718043.2:c.3349T>A XP_006718106.1:p.Leu1117Ile
XM_011540292.1:c.3325T>A XP_011538594.1:p.Leu1109Ile
XR_946029.1:n.1804-102A>T
XM_017016833.1:c.3373T>A XP_016872322.1:p.Leu1125Ile
XM_017016834.2:c.3295T>A XP_016872323.1:p.Leu1099Ile
XM_024448236.1:c.2173T>A XP_024304004.1:p.Leu725Ile
NR_045662.4:n.2832T>A
NR_045663.4:n.3369T>A
NM_001256267.2:c.3295T>A NP_001243196.1:p.Leu1099Ile
NM_001256268.2:c.2413T>A NP_001243197.1:p.Leu805Ile
NM_032578.4:c.3295T>A MANE Select NP_115967.2:p.Leu1099Ile