Canonical Allele Identifier: CA469812342

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959127G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199370G>A , CM000672.2:g.68199370G>A	GRCh38
NC_000010.10:g.69959127G>A , CM000672.1:g.69959127G>A	GRCh37
NC_000010.9:g.69629133G>A	NCBI36
NG_032118.1:g.98254G>A , LRG_410:g.98254G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2463G>A	ENSP00000346369.2:p.Val821=
ENST00000540630.6:c.3342G>A	ENSP00000441668.3:p.Val1114=
ENST00000613327.5:c.3288G>A	ENSP00000480757.2:p.Val1096=
ENST00000688812.1:c.*551G>A	ENSP00000510658.1:n.*551G>A
ENST00000690544.1:c.*2559G>A	ENSP00000508989.1:n.*2559G>A
ENST00000358913.10:c.3288G>A MANE Select	ENSP00000351790.5:p.Val1096=
ENST00000354393.6:c.2463G>A	ENSP00000346369.2:p.Val821=
ENST00000358913.9:c.3288G>A	ENSP00000351790.5:p.Val1096=
ENST00000540630.5:c.3288G>A	ENSP00000441668.2:p.Val1096=
ENST00000613327.4:c.2406G>A	ENSP00000480757.1:p.Val802=
NM_001256267.1:c.3288G>A	NP_001243196.1:p.Val1096=
NM_001256268.1:c.2406G>A	NP_001243197.1:p.Val802=
NM_032578.3:c.3288G>A , LRG_410t1:c.3288G>A	NP_115967.2:p.Val1096=
NR_045662.3:n.2715G>A
NR_045663.3:n.3417G>A
XM_006718043.2:c.3342G>A	XP_006718106.1:p.Val1114=
XM_011540292.1:c.3318G>A	XP_011538594.1:p.Val1106=
XR_946029.1:n.1804-95C>T
XM_017016833.1:c.3366G>A	XP_016872322.1:p.Val1122=
XM_017016834.2:c.3288G>A	XP_016872323.1:p.Val1096=
XM_024448236.1:c.2166G>A	XP_024304004.1:p.Val722=
NR_045662.4:n.2825G>A
NR_045663.4:n.3362G>A
NM_001256267.2:c.3288G>A	NP_001243196.1:p.Val1096=
NM_001256268.2:c.2406G>A	NP_001243197.1:p.Val802=
NM_032578.4:c.3288G>A MANE Select	NP_115967.2:p.Val1096=