Canonical Allele Identifier: CA376840526

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1448566
• ClinVar RCV Id: RCV001980159 ; RCV002407160
• dbSNP Id: rs1226400049
• MyVariant Identifiers: chr10:g.69926314C>T (hg19) ; chr10:g.68166557C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166557C>T , CM000672.2:g.68166557C>T	GRCh38
NC_000010.10:g.69926314C>T , CM000672.1:g.69926314C>T	GRCh37
NC_000010.9:g.69596320C>T	NCBI36
NG_032118.1:g.65441C>T , LRG_410:g.65441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1039C>T	ENSP00000346369.2:p.Gln347Ter
ENST00000373675.4:c.1864C>T	ENSP00000362779.4:p.Gln622Ter
ENST00000540630.6:c.1918C>T	ENSP00000441668.3:p.Gln640Ter
ENST00000613327.5:c.1864C>T	ENSP00000480757.2:p.Gln622Ter
ENST00000687572.1:c.742C>T	ENSP00000510427.1:p.Gln248Ter
ENST00000688812.1:c.1840C>T	ENSP00000510658.1:p.Gln614Ter
ENST00000690544.1:c.*1135C>T	ENSP00000508989.1:n.*1135C>T
ENST00000358913.10:c.1864C>T MANE Select	ENSP00000351790.5:p.Gln622Ter
ENST00000354393.6:c.1039C>T	ENSP00000346369.2:p.Gln347Ter
ENST00000358913.9:c.1864C>T	ENSP00000351790.5:p.Gln622Ter
ENST00000540630.5:c.1864C>T	ENSP00000441668.2:p.Gln622Ter
ENST00000613327.4:c.982C>T	ENSP00000480757.1:p.Gln328Ter
NM_001256267.1:c.1864C>T	NP_001243196.1:p.Gln622Ter
NM_001256268.1:c.982C>T	NP_001243197.1:p.Gln328Ter
NM_032578.3:c.1864C>T , LRG_410t1:c.1864C>T	NP_115967.2:p.Gln622Ter
NR_045662.3:n.1291C>T
NR_045663.3:n.2132C>T
XM_006718043.2:c.1918C>T	XP_006718106.1:p.Gln640Ter
XM_011540292.1:c.1894C>T	XP_011538594.1:p.Gln632Ter
XM_017016833.1:c.1942C>T	XP_016872322.1:p.Gln648Ter
XM_017016834.2:c.1864C>T	XP_016872323.1:p.Gln622Ter
XM_024448236.1:c.742C>T	XP_024304004.1:p.Gln248Ter
NR_045662.4:n.1401C>T
NR_045663.4:n.2077C>T
NM_001256267.2:c.1864C>T	NP_001243196.1:p.Gln622Ter
NM_001256268.2:c.982C>T	NP_001243197.1:p.Gln328Ter
NM_032578.4:c.1864C>T MANE Select	NP_115967.2:p.Gln622Ter