Canonical Allele Identifier: CA469804544

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925466T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165709T>A , CM000672.2:g.68165709T>A	GRCh38
NC_000010.10:g.69925466T>A , CM000672.1:g.69925466T>A	GRCh37
NC_000010.9:g.69595472T>A	NCBI36
NG_032118.1:g.64593T>A , LRG_410:g.64593T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.666T>A	ENSP00000346369.2:p.Ile222=
ENST00000373675.4:c.1491T>A	ENSP00000362779.4:p.Ile497=
ENST00000540630.6:c.1545T>A	ENSP00000441668.3:p.Ile515=
ENST00000613327.5:c.1491T>A	ENSP00000480757.2:p.Ile497=
ENST00000687572.1:c.369T>A	ENSP00000510427.1:p.Ile123=
ENST00000687705.1:c.*1740T>A	ENSP00000509639.1:n.*1740T>A
ENST00000688812.1:c.1467T>A	ENSP00000510658.1:p.Ile489=
ENST00000689002.1:n.543T>A
ENST00000690544.1:c.*762T>A	ENSP00000508989.1:n.*762T>A
ENST00000358913.10:c.1491T>A MANE Select	ENSP00000351790.5:p.Ile497=
ENST00000354393.6:c.666T>A	ENSP00000346369.2:p.Ile222=
ENST00000358913.9:c.1491T>A	ENSP00000351790.5:p.Ile497=
ENST00000540630.5:c.1491T>A	ENSP00000441668.2:p.Ile497=
ENST00000613327.4:c.609T>A	ENSP00000480757.1:p.Ile203=
NM_001256267.1:c.1491T>A	NP_001243196.1:p.Ile497=
NM_001256268.1:c.609T>A	NP_001243197.1:p.Ile203=
NM_032578.3:c.1491T>A , LRG_410t1:c.1491T>A	NP_115967.2:p.Ile497=
NR_045662.3:n.918T>A
NR_045663.3:n.1759T>A
XM_006718043.2:c.1545T>A	XP_006718106.1:p.Ile515=
XM_011540292.1:c.1521T>A	XP_011538594.1:p.Ile507=
XM_017016833.1:c.1569T>A	XP_016872322.1:p.Ile523=
XM_017016834.2:c.1491T>A	XP_016872323.1:p.Ile497=
XM_024448236.1:c.369T>A	XP_024304004.1:p.Ile123=
NR_045662.4:n.1028T>A
NR_045663.4:n.1704T>A
NM_001256267.2:c.1491T>A	NP_001243196.1:p.Ile497=
NM_001256268.2:c.609T>A	NP_001243197.1:p.Ile203=
NM_032578.4:c.1491T>A MANE Select	NP_115967.2:p.Ile497=