Canonical Allele Identifier: CA208195133

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1132410
• ClinVar RCV Id: RCV001466608 ; RCV002368433
• dbSNP Id: rs528450397
• gnomAD v2: 10-69970068-G-A
• gnomAD v3: 10-68210311-G-A
• gnomAD v4: 10-68210311-G-A
• MyVariant Identifiers: chr10:g.69970068G>A (hg19) ; chr10:g.68210311G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210311G>A , CM000672.2:g.68210311G>A	GRCh38
NC_000010.10:g.69970068G>A , CM000672.1:g.69970068G>A	GRCh37
NC_000010.9:g.69640074G>A	NCBI36
NG_032118.1:g.109195G>A , LRG_410:g.109195G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2994G>A	ENSP00000346369.2:p.Pro998=
ENST00000540630.6:c.3873G>A	ENSP00000441668.3:p.Pro1291=
ENST00000613327.5:c.3819G>A	ENSP00000480757.2:p.Pro1273=
ENST00000688812.1:c.*1082G>A	ENSP00000510658.1:n.*1082G>A
ENST00000690544.1:c.*3090G>A	ENSP00000508989.1:n.*3090G>A
ENST00000358913.10:c.3819G>A MANE Select	ENSP00000351790.5:p.Pro1273=
ENST00000354393.6:c.2994G>A	ENSP00000346369.2:p.Pro998=
ENST00000358913.9:c.3819G>A	ENSP00000351790.5:p.Pro1273=
ENST00000540630.5:c.3819G>A	ENSP00000441668.2:p.Pro1273=
ENST00000613327.4:c.2937G>A	ENSP00000480757.1:p.Pro979=
NM_001256267.1:c.3819G>A	NP_001243196.1:p.Pro1273=
NM_001256268.1:c.2937G>A	NP_001243197.1:p.Pro979=
NM_032578.3:c.3819G>A , LRG_410t1:c.3819G>A	NP_115967.2:p.Pro1273=
NR_045662.3:n.3246G>A
NR_045663.3:n.3948G>A
XM_006718043.2:c.3873G>A	XP_006718106.1:p.Pro1291=
XM_011540292.1:c.3849G>A	XP_011538594.1:p.Pro1283=
XR_946029.1:n.1574+4977C>T
XM_017016833.1:c.3897G>A	XP_016872322.1:p.Pro1299=
XM_017016834.2:c.3819G>A	XP_016872323.1:p.Pro1273=
XM_024448236.1:c.2697G>A	XP_024304004.1:p.Pro899=
NR_045662.4:n.3356G>A
NR_045663.4:n.3893G>A
NM_001256267.2:c.3819G>A	NP_001243196.1:p.Pro1273=
NM_001256268.2:c.2937G>A	NP_001243197.1:p.Pro979=
NM_032578.4:c.3819G>A MANE Select	NP_115967.2:p.Pro1273=