Canonical Allele Identifier: CA376839888

Gene: MYPN

Linked Data

• ClinVar Variation Id: 643363
• ClinVar RCV Id: RCV000797046
• dbSNP Id: rs779895608
• gnomAD v4: 10-68166410-C-T
• MyVariant Identifiers: chr10:g.69926167C>T (hg19) ; chr10:g.68166410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166410C>T , CM000672.2:g.68166410C>T	GRCh38
NC_000010.10:g.69926167C>T , CM000672.1:g.69926167C>T	GRCh37
NC_000010.9:g.69596173C>T	NCBI36
NG_032118.1:g.65294C>T , LRG_410:g.65294C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.892C>T	ENSP00000346369.2:p.Pro298Ser
ENST00000373675.4:c.1717C>T	ENSP00000362779.4:p.Pro573Ser
ENST00000540630.6:c.1771C>T	ENSP00000441668.3:p.Pro591Ser
ENST00000613327.5:c.1717C>T	ENSP00000480757.2:p.Pro573Ser
ENST00000687572.1:c.595C>T	ENSP00000510427.1:p.Pro199Ser
ENST00000688812.1:c.1693C>T	ENSP00000510658.1:p.Pro565Ser
ENST00000689002.1:n.769C>T
ENST00000690544.1:c.*988C>T	ENSP00000508989.1:n.*988C>T
ENST00000358913.10:c.1717C>T MANE Select	ENSP00000351790.5:p.Pro573Ser
ENST00000354393.6:c.892C>T	ENSP00000346369.2:p.Pro298Ser
ENST00000358913.9:c.1717C>T	ENSP00000351790.5:p.Pro573Ser
ENST00000540630.5:c.1717C>T	ENSP00000441668.2:p.Pro573Ser
ENST00000613327.4:c.835C>T	ENSP00000480757.1:p.Pro279Ser
NM_001256267.1:c.1717C>T	NP_001243196.1:p.Pro573Ser
NM_001256268.1:c.835C>T	NP_001243197.1:p.Pro279Ser
NM_032578.3:c.1717C>T , LRG_410t1:c.1717C>T	NP_115967.2:p.Pro573Ser
NR_045662.3:n.1144C>T
NR_045663.3:n.1985C>T
XM_006718043.2:c.1771C>T	XP_006718106.1:p.Pro591Ser
XM_011540292.1:c.1747C>T	XP_011538594.1:p.Pro583Ser
XM_017016833.1:c.1795C>T	XP_016872322.1:p.Pro599Ser
XM_017016834.2:c.1717C>T	XP_016872323.1:p.Pro573Ser
XM_024448236.1:c.595C>T	XP_024304004.1:p.Pro199Ser
NR_045662.4:n.1254C>T
NR_045663.4:n.1930C>T
NM_001256267.2:c.1717C>T	NP_001243196.1:p.Pro573Ser
NM_001256268.2:c.835C>T	NP_001243197.1:p.Pro279Ser
NM_032578.4:c.1717C>T MANE Select	NP_115967.2:p.Pro573Ser