Canonical Allele Identifier: CA469812139

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955227C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195470C>A , CM000672.2:g.68195470C>A	GRCh38
NC_000010.10:g.69955227C>A , CM000672.1:g.69955227C>A	GRCh37
NC_000010.9:g.69625233C>A	NCBI36
NG_032118.1:g.94354C>A , LRG_410:g.94354C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2271C>A	ENSP00000346369.2:p.Gly757=
ENST00000540630.6:c.3150C>A	ENSP00000441668.3:p.Gly1050=
ENST00000613327.5:c.3096C>A	ENSP00000480757.2:p.Gly1032=
ENST00000688812.1:c.*359C>A	ENSP00000510658.1:n.*359C>A
ENST00000690544.1:c.*2367C>A	ENSP00000508989.1:n.*2367C>A
ENST00000358913.10:c.3096C>A MANE Select	ENSP00000351790.5:p.Gly1032=
ENST00000354393.6:c.2271C>A	ENSP00000346369.2:p.Gly757=
ENST00000358913.9:c.3096C>A	ENSP00000351790.5:p.Gly1032=
ENST00000540630.5:c.3096C>A	ENSP00000441668.2:p.Gly1032=
ENST00000613327.4:c.2214C>A	ENSP00000480757.1:p.Gly738=
NM_001256267.1:c.3096C>A	NP_001243196.1:p.Gly1032=
NM_001256268.1:c.2214C>A	NP_001243197.1:p.Gly738=
NM_032578.3:c.3096C>A , LRG_410t1:c.3096C>A	NP_115967.2:p.Gly1032=
NR_045662.3:n.2523C>A
NR_045663.3:n.3225C>A
XM_006718043.2:c.3150C>A	XP_006718106.1:p.Gly1050=
XM_011540292.1:c.3126C>A	XP_011538594.1:p.Gly1042=
XM_017016833.1:c.3174C>A	XP_016872322.1:p.Gly1058=
XM_017016834.2:c.3096C>A	XP_016872323.1:p.Gly1032=
XM_024448236.1:c.1974C>A	XP_024304004.1:p.Gly658=
NR_045662.4:n.2633C>A
NR_045663.4:n.3170C>A
NM_001256267.2:c.3096C>A	NP_001243196.1:p.Gly1032=
NM_001256268.2:c.2214C>A	NP_001243197.1:p.Gly738=
NM_032578.4:c.3096C>A MANE Select	NP_115967.2:p.Gly1032=