Canonical Allele Identifier: CA376839338

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926066G>T (hg19) ; chr10:g.68166309G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166309G>T , CM000672.2:g.68166309G>T	GRCh38
NC_000010.10:g.69926066G>T , CM000672.1:g.69926066G>T	GRCh37
NC_000010.9:g.69596072G>T	NCBI36
NG_032118.1:g.65193G>T , LRG_410:g.65193G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.791G>T	ENSP00000346369.2:p.Ser264Ile
ENST00000373675.4:c.1616G>T	ENSP00000362779.4:p.Ser539Ile
ENST00000540630.6:c.1670G>T	ENSP00000441668.3:p.Ser557Ile
ENST00000613327.5:c.1616G>T	ENSP00000480757.2:p.Ser539Ile
ENST00000687572.1:c.494G>T	ENSP00000510427.1:p.Ser165Ile
ENST00000687705.1:c.*1865G>T	ENSP00000509639.1:n.*1865G>T
ENST00000688812.1:c.1592G>T	ENSP00000510658.1:p.Ser531Ile
ENST00000689002.1:n.668G>T
ENST00000690544.1:c.*887G>T	ENSP00000508989.1:n.*887G>T
ENST00000358913.10:c.1616G>T MANE Select	ENSP00000351790.5:p.Ser539Ile
ENST00000354393.6:c.791G>T	ENSP00000346369.2:p.Ser264Ile
ENST00000358913.9:c.1616G>T	ENSP00000351790.5:p.Ser539Ile
ENST00000540630.5:c.1616G>T	ENSP00000441668.2:p.Ser539Ile
ENST00000613327.4:c.734G>T	ENSP00000480757.1:p.Ser245Ile
NM_001256267.1:c.1616G>T	NP_001243196.1:p.Ser539Ile
NM_001256268.1:c.734G>T	NP_001243197.1:p.Ser245Ile
NM_032578.3:c.1616G>T , LRG_410t1:c.1616G>T	NP_115967.2:p.Ser539Ile
NR_045662.3:n.1043G>T
NR_045663.3:n.1884G>T
XM_006718043.2:c.1670G>T	XP_006718106.1:p.Ser557Ile
XM_011540292.1:c.1646G>T	XP_011538594.1:p.Ser549Ile
XM_017016833.1:c.1694G>T	XP_016872322.1:p.Ser565Ile
XM_017016834.2:c.1616G>T	XP_016872323.1:p.Ser539Ile
XM_024448236.1:c.494G>T	XP_024304004.1:p.Ser165Ile
NR_045662.4:n.1153G>T
NR_045663.4:n.1829G>T
NM_001256267.2:c.1616G>T	NP_001243196.1:p.Ser539Ile
NM_001256268.2:c.734G>T	NP_001243197.1:p.Ser245Ile
NM_032578.4:c.1616G>T MANE Select	NP_115967.2:p.Ser539Ile