Canonical Allele Identifier: CA376858103

Gene: MYPN

Linked Data

• dbSNP Id: rs150414382
• gnomAD v2: 10-69957120-G-T
• gnomAD v4: 10-68197363-G-T
• MyVariant Identifiers: chr10:g.69957120G>T (hg19) ; chr10:g.68197363G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197363G>T , CM000672.2:g.68197363G>T	GRCh38
NC_000010.10:g.69957120G>T , CM000672.1:g.69957120G>T	GRCh37
NC_000010.9:g.69627126G>T	NCBI36
NG_032118.1:g.96247G>T , LRG_410:g.96247G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2345G>T	ENSP00000346369.2:p.Arg782Leu
ENST00000540630.6:c.3224G>T	ENSP00000441668.3:p.Arg1075Leu
ENST00000613327.5:c.3170G>T	ENSP00000480757.2:p.Arg1057Leu
ENST00000688812.1:c.*433G>T	ENSP00000510658.1:n.*433G>T
ENST00000690544.1:c.*2441G>T	ENSP00000508989.1:n.*2441G>T
ENST00000358913.10:c.3170G>T MANE Select	ENSP00000351790.5:p.Arg1057Leu
ENST00000354393.6:c.2345G>T	ENSP00000346369.2:p.Arg782Leu
ENST00000358913.9:c.3170G>T	ENSP00000351790.5:p.Arg1057Leu
ENST00000540630.5:c.3170G>T	ENSP00000441668.2:p.Arg1057Leu
ENST00000613327.4:c.2288G>T	ENSP00000480757.1:p.Arg763Leu
NM_001256267.1:c.3170G>T	NP_001243196.1:p.Arg1057Leu
NM_001256268.1:c.2288G>T	NP_001243197.1:p.Arg763Leu
NM_032578.3:c.3170G>T , LRG_410t1:c.3170G>T	NP_115967.2:p.Arg1057Leu
NR_045662.3:n.2597G>T
NR_045663.3:n.3299G>T
XM_006718043.2:c.3224G>T	XP_006718106.1:p.Arg1075Leu
XM_011540292.1:c.3200G>T	XP_011538594.1:p.Arg1067Leu
XM_017016833.1:c.3248G>T	XP_016872322.1:p.Arg1083Leu
XM_017016834.2:c.3170G>T	XP_016872323.1:p.Arg1057Leu
XM_024448236.1:c.2048G>T	XP_024304004.1:p.Arg683Leu
NR_045662.4:n.2707G>T
NR_045663.4:n.3244G>T
NM_001256267.2:c.3170G>T	NP_001243196.1:p.Arg1057Leu
NM_001256268.2:c.2288G>T	NP_001243197.1:p.Arg763Leu
NM_032578.4:c.3170G>T MANE Select	NP_115967.2:p.Arg1057Leu