Canonical Allele Identifier: CA376857508

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955248G>T (hg19) ; chr10:g.68195491G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195491G>T , CM000672.2:g.68195491G>T	GRCh38
NC_000010.10:g.69955248G>T , CM000672.1:g.69955248G>T	GRCh37
NC_000010.9:g.69625254G>T	NCBI36
NG_032118.1:g.94375G>T , LRG_410:g.94375G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2292G>T	ENSP00000346369.2:p.Leu764Phe
ENST00000540630.6:c.3171G>T	ENSP00000441668.3:p.Leu1057Phe
ENST00000613327.5:c.3117G>T	ENSP00000480757.2:p.Leu1039Phe
ENST00000688812.1:c.*380G>T	ENSP00000510658.1:n.*380G>T
ENST00000690544.1:c.*2388G>T	ENSP00000508989.1:n.*2388G>T
ENST00000358913.10:c.3117G>T MANE Select	ENSP00000351790.5:p.Leu1039Phe
ENST00000354393.6:c.2292G>T	ENSP00000346369.2:p.Leu764Phe
ENST00000358913.9:c.3117G>T	ENSP00000351790.5:p.Leu1039Phe
ENST00000540630.5:c.3117G>T	ENSP00000441668.2:p.Leu1039Phe
ENST00000613327.4:c.2235G>T	ENSP00000480757.1:p.Leu745Phe
NM_001256267.1:c.3117G>T	NP_001243196.1:p.Leu1039Phe
NM_001256268.1:c.2235G>T	NP_001243197.1:p.Leu745Phe
NM_032578.3:c.3117G>T , LRG_410t1:c.3117G>T	NP_115967.2:p.Leu1039Phe
NR_045662.3:n.2544G>T
NR_045663.3:n.3246G>T
XM_006718043.2:c.3171G>T	XP_006718106.1:p.Leu1057Phe
XM_011540292.1:c.3147G>T	XP_011538594.1:p.Leu1049Phe
XM_017016833.1:c.3195G>T	XP_016872322.1:p.Leu1065Phe
XM_017016834.2:c.3117G>T	XP_016872323.1:p.Leu1039Phe
XM_024448236.1:c.1995G>T	XP_024304004.1:p.Leu665Phe
NR_045662.4:n.2654G>T
NR_045663.4:n.3191G>T
NM_001256267.2:c.3117G>T	NP_001243196.1:p.Leu1039Phe
NM_001256268.2:c.2235G>T	NP_001243197.1:p.Leu745Phe
NM_032578.4:c.3117G>T MANE Select	NP_115967.2:p.Leu1039Phe