Canonical Allele Identifier: CA376840872

Gene: MYPN

Linked Data

• ClinVar Variation Id: 3012737
• ClinVar RCV Id: RCV003877848
• gnomAD v4: 10-68166617-C-T
• MyVariant Identifiers: chr10:g.69926374C>T (hg19) ; chr10:g.68166617C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166617C>T , CM000672.2:g.68166617C>T	GRCh38
NC_000010.10:g.69926374C>T , CM000672.1:g.69926374C>T	GRCh37
NC_000010.9:g.69596380C>T	NCBI36
NG_032118.1:g.65501C>T , LRG_410:g.65501C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1099C>T	ENSP00000346369.2:p.Pro367Ser
ENST00000373675.4:c.1924C>T	ENSP00000362779.4:p.Pro642Ser
ENST00000540630.6:c.1978C>T	ENSP00000441668.3:p.Pro660Ser
ENST00000613327.5:c.1924C>T	ENSP00000480757.2:p.Pro642Ser
ENST00000687572.1:c.802C>T	ENSP00000510427.1:p.Pro268Ser
ENST00000688812.1:c.1900C>T	ENSP00000510658.1:p.Pro634Ser
ENST00000690544.1:c.*1195C>T	ENSP00000508989.1:n.*1195C>T
ENST00000358913.10:c.1924C>T MANE Select	ENSP00000351790.5:p.Pro642Ser
ENST00000354393.6:c.1099C>T	ENSP00000346369.2:p.Pro367Ser
ENST00000358913.9:c.1924C>T	ENSP00000351790.5:p.Pro642Ser
ENST00000540630.5:c.1924C>T	ENSP00000441668.2:p.Pro642Ser
ENST00000613327.4:c.1042C>T	ENSP00000480757.1:p.Pro348Ser
NM_001256267.1:c.1924C>T	NP_001243196.1:p.Pro642Ser
NM_001256268.1:c.1042C>T	NP_001243197.1:p.Pro348Ser
NM_032578.3:c.1924C>T , LRG_410t1:c.1924C>T	NP_115967.2:p.Pro642Ser
NR_045662.3:n.1351C>T
NR_045663.3:n.2192C>T
XM_006718043.2:c.1978C>T	XP_006718106.1:p.Pro660Ser
XM_011540292.1:c.1954C>T	XP_011538594.1:p.Pro652Ser
XM_017016833.1:c.2002C>T	XP_016872322.1:p.Pro668Ser
XM_017016834.2:c.1924C>T	XP_016872323.1:p.Pro642Ser
XM_024448236.1:c.802C>T	XP_024304004.1:p.Pro268Ser
NR_045662.4:n.1461C>T
NR_045663.4:n.2137C>T
NM_001256267.2:c.1924C>T	NP_001243196.1:p.Pro642Ser
NM_001256268.2:c.1042C>T	NP_001243197.1:p.Pro348Ser
NM_032578.4:c.1924C>T MANE Select	NP_115967.2:p.Pro642Ser