Canonical Allele Identifier: CA376859226

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959234T>A (hg19) ; chr10:g.68199477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199477T>A , CM000672.2:g.68199477T>A	GRCh38
NC_000010.10:g.69959234T>A , CM000672.1:g.69959234T>A	GRCh37
NC_000010.9:g.69629240T>A	NCBI36
NG_032118.1:g.98361T>A , LRG_410:g.98361T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2570T>A	ENSP00000346369.2:p.Leu857His
ENST00000540630.6:c.3449T>A	ENSP00000441668.3:p.Leu1150His
ENST00000613327.5:c.3395T>A	ENSP00000480757.2:p.Leu1132His
ENST00000688812.1:c.*658T>A	ENSP00000510658.1:n.*658T>A
ENST00000690544.1:c.*2666T>A	ENSP00000508989.1:n.*2666T>A
ENST00000358913.10:c.3395T>A MANE Select	ENSP00000351790.5:p.Leu1132His
ENST00000354393.6:c.2570T>A	ENSP00000346369.2:p.Leu857His
ENST00000358913.9:c.3395T>A	ENSP00000351790.5:p.Leu1132His
ENST00000540630.5:c.3395T>A	ENSP00000441668.2:p.Leu1132His
ENST00000613327.4:c.2513T>A	ENSP00000480757.1:p.Leu838His
NM_001256267.1:c.3395T>A	NP_001243196.1:p.Leu1132His
NM_001256268.1:c.2513T>A	NP_001243197.1:p.Leu838His
NM_032578.3:c.3395T>A , LRG_410t1:c.3395T>A	NP_115967.2:p.Leu1132His
NR_045662.3:n.2822T>A
NR_045663.3:n.3524T>A
XM_006718043.2:c.3449T>A	XP_006718106.1:p.Leu1150His
XM_011540292.1:c.3425T>A	XP_011538594.1:p.Leu1142His
XR_946029.1:n.1804-202A>T
XM_017016833.1:c.3473T>A	XP_016872322.1:p.Leu1158His
XM_017016834.2:c.3395T>A	XP_016872323.1:p.Leu1132His
XM_024448236.1:c.2273T>A	XP_024304004.1:p.Leu758His
NR_045662.4:n.2932T>A
NR_045663.4:n.3469T>A
NM_001256267.2:c.3395T>A	NP_001243196.1:p.Leu1132His
NM_001256268.2:c.2513T>A	NP_001243197.1:p.Leu838His
NM_032578.4:c.3395T>A MANE Select	NP_115967.2:p.Leu1132His