Canonical Allele Identifier: CA376858942

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959150T>A (hg19) ; chr10:g.68199393T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199393T>A , CM000672.2:g.68199393T>A	GRCh38
NC_000010.10:g.69959150T>A , CM000672.1:g.69959150T>A	GRCh37
NC_000010.9:g.69629156T>A	NCBI36
NG_032118.1:g.98277T>A , LRG_410:g.98277T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2486T>A	ENSP00000346369.2:p.Leu829Gln
ENST00000540630.6:c.3365T>A	ENSP00000441668.3:p.Leu1122Gln
ENST00000613327.5:c.3311T>A	ENSP00000480757.2:p.Leu1104Gln
ENST00000688812.1:c.*574T>A	ENSP00000510658.1:n.*574T>A
ENST00000690544.1:c.*2582T>A	ENSP00000508989.1:n.*2582T>A
ENST00000358913.10:c.3311T>A MANE Select	ENSP00000351790.5:p.Leu1104Gln
ENST00000354393.6:c.2486T>A	ENSP00000346369.2:p.Leu829Gln
ENST00000358913.9:c.3311T>A	ENSP00000351790.5:p.Leu1104Gln
ENST00000540630.5:c.3311T>A	ENSP00000441668.2:p.Leu1104Gln
ENST00000613327.4:c.2429T>A	ENSP00000480757.1:p.Leu810Gln
NM_001256267.1:c.3311T>A	NP_001243196.1:p.Leu1104Gln
NM_001256268.1:c.2429T>A	NP_001243197.1:p.Leu810Gln
NM_032578.3:c.3311T>A , LRG_410t1:c.3311T>A	NP_115967.2:p.Leu1104Gln
NR_045662.3:n.2738T>A
NR_045663.3:n.3440T>A
XM_006718043.2:c.3365T>A	XP_006718106.1:p.Leu1122Gln
XM_011540292.1:c.3341T>A	XP_011538594.1:p.Leu1114Gln
XR_946029.1:n.1804-118A>T
XM_017016833.1:c.3389T>A	XP_016872322.1:p.Leu1130Gln
XM_017016834.2:c.3311T>A	XP_016872323.1:p.Leu1104Gln
XM_024448236.1:c.2189T>A	XP_024304004.1:p.Leu730Gln
NR_045662.4:n.2848T>A
NR_045663.4:n.3385T>A
NM_001256267.2:c.3311T>A	NP_001243196.1:p.Leu1104Gln
NM_001256268.2:c.2429T>A	NP_001243197.1:p.Leu810Gln
NM_032578.4:c.3311T>A MANE Select	NP_115967.2:p.Leu1104Gln