Canonical Allele Identifier: CA376840670

Gene: MYPN

Linked Data

• gnomAD v3: 10-68166587-T-A
• gnomAD v4: 10-68166587-T-A
• MyVariant Identifiers: chr10:g.69926344T>A (hg19) ; chr10:g.68166587T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166587T>A , CM000672.2:g.68166587T>A	GRCh38
NC_000010.10:g.69926344T>A , CM000672.1:g.69926344T>A	GRCh37
NC_000010.9:g.69596350T>A	NCBI36
NG_032118.1:g.65471T>A , LRG_410:g.65471T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1069T>A	ENSP00000346369.2:p.Phe357Ile
ENST00000373675.4:c.1894T>A	ENSP00000362779.4:p.Phe632Ile
ENST00000540630.6:c.1948T>A	ENSP00000441668.3:p.Phe650Ile
ENST00000613327.5:c.1894T>A	ENSP00000480757.2:p.Phe632Ile
ENST00000687572.1:c.772T>A	ENSP00000510427.1:p.Phe258Ile
ENST00000688812.1:c.1870T>A	ENSP00000510658.1:p.Phe624Ile
ENST00000690544.1:c.*1165T>A	ENSP00000508989.1:n.*1165T>A
ENST00000358913.10:c.1894T>A MANE Select	ENSP00000351790.5:p.Phe632Ile
ENST00000354393.6:c.1069T>A	ENSP00000346369.2:p.Phe357Ile
ENST00000358913.9:c.1894T>A	ENSP00000351790.5:p.Phe632Ile
ENST00000540630.5:c.1894T>A	ENSP00000441668.2:p.Phe632Ile
ENST00000613327.4:c.1012T>A	ENSP00000480757.1:p.Phe338Ile
NM_001256267.1:c.1894T>A	NP_001243196.1:p.Phe632Ile
NM_001256268.1:c.1012T>A	NP_001243197.1:p.Phe338Ile
NM_032578.3:c.1894T>A , LRG_410t1:c.1894T>A	NP_115967.2:p.Phe632Ile
NR_045662.3:n.1321T>A
NR_045663.3:n.2162T>A
XM_006718043.2:c.1948T>A	XP_006718106.1:p.Phe650Ile
XM_011540292.1:c.1924T>A	XP_011538594.1:p.Phe642Ile
XM_017016833.1:c.1972T>A	XP_016872322.1:p.Phe658Ile
XM_017016834.2:c.1894T>A	XP_016872323.1:p.Phe632Ile
XM_024448236.1:c.772T>A	XP_024304004.1:p.Phe258Ile
NR_045662.4:n.1431T>A
NR_045663.4:n.2107T>A
NM_001256267.2:c.1894T>A	NP_001243196.1:p.Phe632Ile
NM_001256268.2:c.1012T>A	NP_001243197.1:p.Phe338Ile
NM_032578.4:c.1894T>A MANE Select	NP_115967.2:p.Phe632Ile