Canonical Allele Identifier: CA376841170

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926422C>T (hg19) ; chr10:g.68166665C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166665C>T , CM000672.2:g.68166665C>T	GRCh38
NC_000010.10:g.69926422C>T , CM000672.1:g.69926422C>T	GRCh37
NC_000010.9:g.69596428C>T	NCBI36
NG_032118.1:g.65549C>T , LRG_410:g.65549C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1147C>T	ENSP00000346369.2:p.Leu383Phe
ENST00000373675.4:c.1972C>T	ENSP00000362779.4:p.Leu658=
ENST00000540630.6:c.2026C>T	ENSP00000441668.3:p.Leu676Phe
ENST00000613327.5:c.1972C>T	ENSP00000480757.2:p.Leu658Phe
ENST00000687572.1:c.850C>T
ENST00000688812.1:c.1948C>T	ENSP00000510658.1:p.Leu650Phe
ENST00000690544.1:c.*1243C>T	ENSP00000508989.1:n.*1243C>T
ENST00000358913.10:c.1972C>T MANE Select	ENSP00000351790.5:p.Leu658Phe
ENST00000354393.6:c.1147C>T	ENSP00000346369.2:p.Leu383Phe
ENST00000358913.9:c.1972C>T	ENSP00000351790.5:p.Leu658Phe
ENST00000540630.5:c.1972C>T	ENSP00000441668.2:p.Leu658Phe
ENST00000613327.4:c.1090C>T	ENSP00000480757.1:p.Leu364Phe
NM_001256267.1:c.1972C>T	NP_001243196.1:p.Leu658Phe
NM_001256268.1:c.1090C>T	NP_001243197.1:p.Leu364Phe
NM_032578.3:c.1972C>T , LRG_410t1:c.1972C>T	NP_115967.2:p.Leu658Phe
NR_045662.3:n.1399C>T
NR_045663.3:n.2240C>T
XM_006718043.2:c.2026C>T	XP_006718106.1:p.Leu676Phe
XM_011540292.1:c.2002C>T	XP_011538594.1:p.Leu668Phe
XM_017016833.1:c.2050C>T	XP_016872322.1:p.Leu684Phe
XM_017016834.2:c.1972C>T	XP_016872323.1:p.Leu658Phe
XM_024448236.1:c.850C>T	XP_024304004.1:p.Leu284Phe
NR_045662.4:n.1509C>T
NR_045663.4:n.2185C>T
NM_001256267.2:c.1972C>T	NP_001243196.1:p.Leu658Phe
NM_001256268.2:c.1090C>T	NP_001243197.1:p.Leu364Phe
NM_032578.4:c.1972C>T MANE Select	NP_115967.2:p.Leu658Phe