Canonical Allele Identifier: CA376840870

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926374C>A (hg19) ; chr10:g.68166617C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1099C>A	ENSP00000346369.2:p.Pro367Thr
ENST00000373675.4:c.1924C>A	ENSP00000362779.4:p.Pro642Thr
ENST00000540630.6:c.1978C>A	ENSP00000441668.3:p.Pro660Thr
ENST00000613327.5:c.1924C>A	ENSP00000480757.2:p.Pro642Thr
ENST00000687572.1:c.802C>A	ENSP00000510427.1:p.Pro268Thr
ENST00000688812.1:c.1900C>A	ENSP00000510658.1:p.Pro634Thr
ENST00000690544.1:c.*1195C>A	ENSP00000508989.1:n.*1195C>A
ENST00000358913.10:c.1924C>A MANE Select	ENSP00000351790.5:p.Pro642Thr
ENST00000354393.6:c.1099C>A	ENSP00000346369.2:p.Pro367Thr
ENST00000358913.9:c.1924C>A	ENSP00000351790.5:p.Pro642Thr
ENST00000540630.5:c.1924C>A	ENSP00000441668.2:p.Pro642Thr
ENST00000613327.4:c.1042C>A	ENSP00000480757.1:p.Pro348Thr
NM_001256267.1:c.1924C>A	NP_001243196.1:p.Pro642Thr
NM_001256268.1:c.1042C>A	NP_001243197.1:p.Pro348Thr
NM_032578.3:c.1924C>A , LRG_410t1:c.1924C>A	NP_115967.2:p.Pro642Thr
NR_045662.3:n.1351C>A
NR_045663.3:n.2192C>A
XM_006718043.2:c.1978C>A	XP_006718106.1:p.Pro660Thr
XM_011540292.1:c.1954C>A	XP_011538594.1:p.Pro652Thr
XM_017016833.1:c.2002C>A	XP_016872322.1:p.Pro668Thr
XM_017016834.2:c.1924C>A	XP_016872323.1:p.Pro642Thr
XM_024448236.1:c.802C>A	XP_024304004.1:p.Pro268Thr
NR_045662.4:n.1461C>A
NR_045663.4:n.2137C>A
NM_001256267.2:c.1924C>A	NP_001243196.1:p.Pro642Thr
NM_001256268.2:c.1042C>A	NP_001243197.1:p.Pro348Thr
NM_032578.4:c.1924C>A MANE Select	NP_115967.2:p.Pro642Thr