Canonical Allele Identifier: CA469812446

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199466C>T , CM000672.2:g.68199466C>T	GRCh38
NC_000010.10:g.69959223C>T , CM000672.1:g.69959223C>T	GRCh37
NC_000010.9:g.69629229C>T	NCBI36
NG_032118.1:g.98350C>T , LRG_410:g.98350C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3384C>T MANE Select	NP_115967.2:p.Val1128=
ENST00000358913.10:c.3384C>T MANE Select	ENSP00000351790.5:p.Val1128=
NM_001256267.1:c.3384C>T	NP_001243196.1:p.Val1128=
NM_001256267.2:c.3384C>T	NP_001243196.1:p.Val1128=
NM_001256268.1:c.2502C>T	NP_001243197.1:p.Val834=
NM_001256268.2:c.2502C>T	NP_001243197.1:p.Val834=
NM_032578.3:c.3384C>T , LRG_410t1:c.3384C>T	NP_115967.2:p.Val1128=
NR_045662.3:n.2811C>T
NR_045662.4:n.2921C>T
NR_045663.3:n.3513C>T
NR_045663.4:n.3458C>T
ENST00000354393.6:c.2559C>T	ENSP00000346369.2:p.Val853=
ENST00000354393.7:c.2559C>T	ENSP00000346369.2:p.Val853=
ENST00000358913.9:c.3384C>T	ENSP00000351790.5:p.Val1128=
ENST00000540630.5:c.3384C>T	ENSP00000441668.2:p.Val1128=
ENST00000540630.6:c.3438C>T	ENSP00000441668.3:p.Val1146=
ENST00000613327.4:c.2502C>T	ENSP00000480757.1:p.Val834=
ENST00000613327.5:c.3384C>T	ENSP00000480757.2:p.Val1128=
ENST00000688812.1:c.*647C>T	ENSP00000510658.1:n.*647C>T
ENST00000690544.1:c.*2655C>T	ENSP00000508989.1:n.*2655C>T
XM_006718043.2:c.3438C>T	XP_006718106.1:p.Val1146=
XM_011540292.1:c.3414C>T	XP_011538594.1:p.Val1138=
XM_017016833.1:c.3462C>T	XP_016872322.1:p.Val1154=
XM_017016834.2:c.3384C>T	XP_016872323.1:p.Val1128=
XM_024448236.1:c.2262C>T	XP_024304004.1:p.Val754=
XR_946029.1:n.1804-191G>A