Canonical Allele Identifier: CA376839820

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926152C>T (hg19) ; chr10:g.68166395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166395C>T , CM000672.2:g.68166395C>T	GRCh38
NC_000010.10:g.69926152C>T , CM000672.1:g.69926152C>T	GRCh37
NC_000010.9:g.69596158C>T	NCBI36
NG_032118.1:g.65279C>T , LRG_410:g.65279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.877C>T	ENSP00000346369.2:p.Pro293Ser
ENST00000373675.4:c.1702C>T	ENSP00000362779.4:p.Pro568Ser
ENST00000540630.6:c.1756C>T	ENSP00000441668.3:p.Pro586Ser
ENST00000613327.5:c.1702C>T	ENSP00000480757.2:p.Pro568Ser
ENST00000687572.1:c.580C>T	ENSP00000510427.1:p.Pro194Ser
ENST00000688812.1:c.1678C>T	ENSP00000510658.1:p.Pro560Ser
ENST00000689002.1:n.754C>T
ENST00000690544.1:c.*973C>T	ENSP00000508989.1:n.*973C>T
ENST00000358913.10:c.1702C>T MANE Select	ENSP00000351790.5:p.Pro568Ser
ENST00000354393.6:c.877C>T	ENSP00000346369.2:p.Pro293Ser
ENST00000358913.9:c.1702C>T	ENSP00000351790.5:p.Pro568Ser
ENST00000540630.5:c.1702C>T	ENSP00000441668.2:p.Pro568Ser
ENST00000613327.4:c.820C>T	ENSP00000480757.1:p.Pro274Ser
NM_001256267.1:c.1702C>T	NP_001243196.1:p.Pro568Ser
NM_001256268.1:c.820C>T	NP_001243197.1:p.Pro274Ser
NM_032578.3:c.1702C>T , LRG_410t1:c.1702C>T	NP_115967.2:p.Pro568Ser
NR_045662.3:n.1129C>T
NR_045663.3:n.1970C>T
XM_006718043.2:c.1756C>T	XP_006718106.1:p.Pro586Ser
XM_011540292.1:c.1732C>T	XP_011538594.1:p.Pro578Ser
XM_017016833.1:c.1780C>T	XP_016872322.1:p.Pro594Ser
XM_017016834.2:c.1702C>T	XP_016872323.1:p.Pro568Ser
XM_024448236.1:c.580C>T	XP_024304004.1:p.Pro194Ser
NR_045662.4:n.1239C>T
NR_045663.4:n.1915C>T
NM_001256267.2:c.1702C>T	NP_001243196.1:p.Pro568Ser
NM_001256268.2:c.820C>T	NP_001243197.1:p.Pro274Ser
NM_032578.4:c.1702C>T MANE Select	NP_115967.2:p.Pro568Ser