Canonical Allele Identifier: CA5523237

Gene: MYPN

Linked Data

• dbSNP Id: rs537970618
• ExAC: 10:69970402 G / T
• gnomAD v2: 10-69970402-G-T
• gnomAD v3: 10-68210645-G-T
• gnomAD v4: 10-68210645-G-T
• MyVariant Identifiers: chr10:g.69970402G>T (hg19) ; chr10:g.68210645G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210645G>T , CM000672.2:g.68210645G>T	GRCh38
NC_000010.10:g.69970402G>T , CM000672.1:g.69970402G>T	GRCh37
NC_000010.9:g.69640408G>T	NCBI36
NG_032118.1:g.109529G>T , LRG_410:g.109529G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*190G>T	ENSP00000346369.2:n.*190G>T
ENST00000540630.6:c.*190G>T	ENSP00000441668.3:n.*190G>T
ENST00000613327.5:c.*190G>T	ENSP00000480757.2:n.*190G>T
ENST00000688812.1:c.*1416G>T	ENSP00000510658.1:n.*1416G>T
ENST00000690544.1:c.*3424G>T	ENSP00000508989.1:n.*3424G>T
ENST00000358913.10:c.*190G>T MANE Select	ENSP00000351790.5:n.*190G>T
ENST00000354393.6:c.*190G>T	ENSP00000346369.2:n.*190G>T
ENST00000358913.9:c.*190G>T	ENSP00000351790.5:n.*190G>T
ENST00000540630.5:c.*190G>T	ENSP00000441668.2:n.*190G>T
ENST00000613327.4:c.*190G>T	ENSP00000480757.1:n.*190G>T
NM_001256267.1:c.*190G>T	NP_001243196.1:n.*190G>T
NM_001256268.1:c.*190G>T	NP_001243197.1:n.*190G>T
NM_032578.3:c.*190G>T , LRG_410t1:c.*190G>T	NP_115967.2:n.*190G>T
NR_045662.3:n.3580G>T
NR_045663.3:n.4282G>T
XM_006718043.2:c.*190G>T	XP_006718106.1:n.*190G>T
XM_011540292.1:c.*190G>T	XP_011538594.1:n.*190G>T
XR_946029.1:n.1574+4643C>A
XM_017016833.1:c.*190G>T	XP_016872322.1:n.*190G>T
XM_017016834.2:c.*190G>T	XP_016872323.1:n.*190G>T
XM_024448236.1:c.*190G>T	XP_024304004.1:n.*190G>T
NR_045662.4:n.3690G>T
NR_045663.4:n.4227G>T
NM_001256267.2:c.*190G>T	NP_001243196.1:n.*190G>T
NM_001256268.2:c.*190G>T	NP_001243197.1:n.*190G>T
NM_032578.4:c.*190G>T MANE Select	NP_115967.2:n.*190G>T