Canonical Allele Identifier: CA376859219
Gene: MYPN HGNC NCBI

Linked Data

dbSNP Id: rs1238852443

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199474T>C , CM000672.2:g.68199474T>C GRCh38
NC_000010.10:g.69959231T>C , CM000672.1:g.69959231T>C GRCh37
NC_000010.9:g.69629237T>C NCBI36
NG_032118.1:g.98358T>C , LRG_410:g.98358T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2567T>C ENSP00000346369.2:p.Leu856Pro
ENST00000540630.6:c.3446T>C ENSP00000441668.3:p.Leu1149Pro
ENST00000613327.5:c.3392T>C ENSP00000480757.2:p.Leu1131Pro
ENST00000688812.1:c.*655T>C ENSP00000510658.1:n.*655T>C
ENST00000690544.1:c.*2663T>C ENSP00000508989.1:n.*2663T>C
ENST00000358913.10:c.3392T>C MANE Select ENSP00000351790.5:p.Leu1131Pro
ENST00000354393.6:c.2567T>C ENSP00000346369.2:p.Leu856Pro
ENST00000358913.9:c.3392T>C ENSP00000351790.5:p.Leu1131Pro
ENST00000540630.5:c.3392T>C ENSP00000441668.2:p.Leu1131Pro
ENST00000613327.4:c.2510T>C ENSP00000480757.1:p.Leu837Pro
NM_001256267.1:c.3392T>C NP_001243196.1:p.Leu1131Pro
NM_001256268.1:c.2510T>C NP_001243197.1:p.Leu837Pro
NM_032578.3:c.3392T>C , LRG_410t1:c.3392T>C NP_115967.2:p.Leu1131Pro
NR_045662.3:n.2819T>C
NR_045663.3:n.3521T>C
XM_006718043.2:c.3446T>C XP_006718106.1:p.Leu1149Pro
XM_011540292.1:c.3422T>C XP_011538594.1:p.Leu1141Pro
XR_946029.1:n.1804-199A>G
XM_017016833.1:c.3470T>C XP_016872322.1:p.Leu1157Pro
XM_017016834.2:c.3392T>C XP_016872323.1:p.Leu1131Pro
XM_024448236.1:c.2270T>C XP_024304004.1:p.Leu757Pro
NR_045662.4:n.2929T>C
NR_045663.4:n.3466T>C
NM_001256267.2:c.3392T>C NP_001243196.1:p.Leu1131Pro
NM_001256268.2:c.2510T>C NP_001243197.1:p.Leu837Pro
NM_032578.4:c.3392T>C MANE Select NP_115967.2:p.Leu1131Pro