Canonical Allele Identifier: CA376857739

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955280A>T (hg19) ; chr10:g.68195523A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195523A>T , CM000672.2:g.68195523A>T	GRCh38
NC_000010.10:g.69955280A>T , CM000672.1:g.69955280A>T	GRCh37
NC_000010.9:g.69625286A>T	NCBI36
NG_032118.1:g.94407A>T , LRG_410:g.94407A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2324A>T	ENSP00000346369.2:p.Gln775Leu
ENST00000540630.6:c.3203A>T	ENSP00000441668.3:p.Gln1068Leu
ENST00000613327.5:c.3149A>T	ENSP00000480757.2:p.Gln1050Leu
ENST00000688812.1:c.*412A>T	ENSP00000510658.1:n.*412A>T
ENST00000690544.1:c.*2420A>T	ENSP00000508989.1:n.*2420A>T
ENST00000358913.10:c.3149A>T MANE Select	ENSP00000351790.5:p.Gln1050Leu
ENST00000354393.6:c.2324A>T	ENSP00000346369.2:p.Gln775Leu
ENST00000358913.9:c.3149A>T	ENSP00000351790.5:p.Gln1050Leu
ENST00000540630.5:c.3149A>T	ENSP00000441668.2:p.Gln1050Leu
ENST00000613327.4:c.2267A>T	ENSP00000480757.1:p.Gln756Leu
NM_001256267.1:c.3149A>T	NP_001243196.1:p.Gln1050Leu
NM_001256268.1:c.2267A>T	NP_001243197.1:p.Gln756Leu
NM_032578.3:c.3149A>T , LRG_410t1:c.3149A>T	NP_115967.2:p.Gln1050Leu
NR_045662.3:n.2576A>T
NR_045663.3:n.3278A>T
XM_006718043.2:c.3203A>T	XP_006718106.1:p.Gln1068Leu
XM_011540292.1:c.3179A>T	XP_011538594.1:p.Gln1060Leu
XM_017016833.1:c.3227A>T	XP_016872322.1:p.Gln1076Leu
XM_017016834.2:c.3149A>T	XP_016872323.1:p.Gln1050Leu
XM_024448236.1:c.2027A>T	XP_024304004.1:p.Gln676Leu
NR_045662.4:n.2686A>T
NR_045663.4:n.3223A>T
NM_001256267.2:c.3149A>T	NP_001243196.1:p.Gln1050Leu
NM_001256268.2:c.2267A>T	NP_001243197.1:p.Gln756Leu
NM_032578.4:c.3149A>T MANE Select	NP_115967.2:p.Gln1050Leu