Canonical Allele Identifier: CA2609374259

Gene: MYPN

Linked Data

• gnomAD v4: 10-68210597-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210597C>T , CM000672.2:g.68210597C>T	GRCh38
NC_000010.10:g.69970354C>T , CM000672.1:g.69970354C>T	GRCh37
NC_000010.9:g.69640360C>T	NCBI36
NG_032118.1:g.109481C>T , LRG_410:g.109481C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*142C>T	ENSP00000346369.2:n.*142C>T
ENST00000540630.6:c.*142C>T	ENSP00000441668.3:n.*142C>T
ENST00000613327.5:c.*142C>T	ENSP00000480757.2:n.*142C>T
ENST00000688812.1:c.*1368C>T	ENSP00000510658.1:n.*1368C>T
ENST00000690544.1:c.*3376C>T	ENSP00000508989.1:n.*3376C>T
ENST00000358913.10:c.*142C>T MANE Select	ENSP00000351790.5:n.*142C>T
ENST00000354393.6:c.*142C>T	ENSP00000346369.2:n.*142C>T
ENST00000358913.9:c.*142C>T	ENSP00000351790.5:n.*142C>T
ENST00000540630.5:c.*142C>T	ENSP00000441668.2:n.*142C>T
ENST00000613327.4:c.*142C>T	ENSP00000480757.1:n.*142C>T
NM_001256267.1:c.*142C>T	NP_001243196.1:n.*142C>T
NM_001256268.1:c.*142C>T	NP_001243197.1:n.*142C>T
NM_032578.3:c.*142C>T , LRG_410t1:c.*142C>T	NP_115967.2:n.*142C>T
NR_045662.3:n.3532C>T
NR_045663.3:n.4234C>T
XM_006718043.2:c.*142C>T	XP_006718106.1:n.*142C>T
XM_011540292.1:c.*142C>T	XP_011538594.1:n.*142C>T
XR_946029.1:n.1574+4691G>A
XM_017016833.1:c.*142C>T	XP_016872322.1:n.*142C>T
XM_017016834.2:c.*142C>T	XP_016872323.1:n.*142C>T
XM_024448236.1:c.*142C>T	XP_024304004.1:n.*142C>T
NR_045662.4:n.3642C>T
NR_045663.4:n.4179C>T
NM_001256267.2:c.*142C>T	NP_001243196.1:n.*142C>T
NM_001256268.2:c.*142C>T	NP_001243197.1:n.*142C>T
NM_032578.4:c.*142C>T MANE Select	NP_115967.2:n.*142C>T