Canonical Allele Identifier: CA376857415

Gene: MYPN

Linked Data

• ClinVar Variation Id: 2412857
• ClinVar RCV Id: RCV003109872
• gnomAD v4: 10-68195480-G-A
• MyVariant Identifiers: chr10:g.69955237G>A (hg19) ; chr10:g.68195480G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195480G>A , CM000672.2:g.68195480G>A	GRCh38
NC_000010.10:g.69955237G>A , CM000672.1:g.69955237G>A	GRCh37
NC_000010.9:g.69625243G>A	NCBI36
NG_032118.1:g.94364G>A , LRG_410:g.94364G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2281G>A	ENSP00000346369.2:p.Val761Ile
ENST00000540630.6:c.3160G>A	ENSP00000441668.3:p.Val1054Ile
ENST00000613327.5:c.3106G>A	ENSP00000480757.2:p.Val1036Ile
ENST00000688812.1:c.*369G>A	ENSP00000510658.1:n.*369G>A
ENST00000690544.1:c.*2377G>A	ENSP00000508989.1:n.*2377G>A
ENST00000358913.10:c.3106G>A MANE Select	ENSP00000351790.5:p.Val1036Ile
ENST00000354393.6:c.2281G>A	ENSP00000346369.2:p.Val761Ile
ENST00000358913.9:c.3106G>A	ENSP00000351790.5:p.Val1036Ile
ENST00000540630.5:c.3106G>A	ENSP00000441668.2:p.Val1036Ile
ENST00000613327.4:c.2224G>A	ENSP00000480757.1:p.Val742Ile
NM_001256267.1:c.3106G>A	NP_001243196.1:p.Val1036Ile
NM_001256268.1:c.2224G>A	NP_001243197.1:p.Val742Ile
NM_032578.3:c.3106G>A , LRG_410t1:c.3106G>A	NP_115967.2:p.Val1036Ile
NR_045662.3:n.2533G>A
NR_045663.3:n.3235G>A
XM_006718043.2:c.3160G>A	XP_006718106.1:p.Val1054Ile
XM_011540292.1:c.3136G>A	XP_011538594.1:p.Val1046Ile
XM_017016833.1:c.3184G>A	XP_016872322.1:p.Val1062Ile
XM_017016834.2:c.3106G>A	XP_016872323.1:p.Val1036Ile
XM_024448236.1:c.1984G>A	XP_024304004.1:p.Val662Ile
NR_045662.4:n.2643G>A
NR_045663.4:n.3180G>A
NM_001256267.2:c.3106G>A	NP_001243196.1:p.Val1036Ile
NM_001256268.2:c.2224G>A	NP_001243197.1:p.Val742Ile
NM_032578.4:c.3106G>A MANE Select	NP_115967.2:p.Val1036Ile