Canonical Allele Identifier: CA333124

Gene: MYPN

Linked Data

• ClinVar Variation Id: 138423
• ClinVar RCV Id: RCV000127081 ; RCV000230996 ; RCV000621053
• dbSNP Id: rs114479328
• ExAC: 10:69955209 G / A
• gnomAD v2: 10-69955209-G-A
• gnomAD v3: 10-68195452-G-A
• gnomAD v4: 10-68195452-G-A
• MyVariant Identifiers: chr10:g.69955209G>A (hg19) ; chr10:g.68195452G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195452G>A , CM000672.2:g.68195452G>A	GRCh38
NC_000010.10:g.69955209G>A , CM000672.1:g.69955209G>A	GRCh37
NC_000010.9:g.69625215G>A	NCBI36
NG_032118.1:g.94336G>A , LRG_410:g.94336G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2253G>A	ENSP00000346369.2:p.Gly751=
ENST00000540630.6:c.3132G>A	ENSP00000441668.3:p.Gly1044=
ENST00000613327.5:c.3078G>A	ENSP00000480757.2:p.Gly1026=
ENST00000688812.1:c.*341G>A	ENSP00000510658.1:n.*341G>A
ENST00000690544.1:c.*2349G>A	ENSP00000508989.1:n.*2349G>A
ENST00000358913.10:c.3078G>A MANE Select	ENSP00000351790.5:p.Gly1026=
ENST00000354393.6:c.2253G>A	ENSP00000346369.2:p.Gly751=
ENST00000358913.9:c.3078G>A	ENSP00000351790.5:p.Gly1026=
ENST00000540630.5:c.3078G>A	ENSP00000441668.2:p.Gly1026=
ENST00000613327.4:c.2196G>A	ENSP00000480757.1:p.Gly732=
NM_001256267.1:c.3078G>A	NP_001243196.1:p.Gly1026=
NM_001256268.1:c.2196G>A	NP_001243197.1:p.Gly732=
NM_032578.3:c.3078G>A , LRG_410t1:c.3078G>A	NP_115967.2:p.Gly1026=
NR_045662.3:n.2505G>A
NR_045663.3:n.3207G>A
XM_006718043.2:c.3132G>A	XP_006718106.1:p.Gly1044=
XM_011540292.1:c.3108G>A	XP_011538594.1:p.Gly1036=
XM_017016833.1:c.3156G>A	XP_016872322.1:p.Gly1052=
XM_017016834.2:c.3078G>A	XP_016872323.1:p.Gly1026=
XM_024448236.1:c.1956G>A	XP_024304004.1:p.Gly652=
NR_045662.4:n.2615G>A
NR_045663.4:n.3152G>A
NM_001256267.2:c.3078G>A	NP_001243196.1:p.Gly1026=
NM_001256268.2:c.2196G>A	NP_001243197.1:p.Gly732=
NM_032578.4:c.3078G>A MANE Select	NP_115967.2:p.Gly1026=