Canonical Allele Identifier: CA376840605

Gene: MYPN

Linked Data

• ClinVar Variation Id: 520317
• ClinVar RCV Id: RCV000618459 ; RCV001231665
• dbSNP Id: rs1282443178
• gnomAD v3: 10-68166572-T-A
• gnomAD v4: 10-68166572-T-A
• MyVariant Identifiers: chr10:g.69926329T>A (hg19) ; chr10:g.68166572T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166572T>A , CM000672.2:g.68166572T>A	GRCh38
NC_000010.10:g.69926329T>A , CM000672.1:g.69926329T>A	GRCh37
NC_000010.9:g.69596335T>A	NCBI36
NG_032118.1:g.65456T>A , LRG_410:g.65456T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1054T>A	ENSP00000346369.2:p.Ser352Thr
ENST00000373675.4:c.1879T>A	ENSP00000362779.4:p.Ser627Thr
ENST00000540630.6:c.1933T>A	ENSP00000441668.3:p.Ser645Thr
ENST00000613327.5:c.1879T>A	ENSP00000480757.2:p.Ser627Thr
ENST00000687572.1:c.757T>A	ENSP00000510427.1:p.Ser253Thr
ENST00000688812.1:c.1855T>A	ENSP00000510658.1:p.Ser619Thr
ENST00000690544.1:c.*1150T>A	ENSP00000508989.1:n.*1150T>A
ENST00000358913.10:c.1879T>A MANE Select	ENSP00000351790.5:p.Ser627Thr
ENST00000354393.6:c.1054T>A	ENSP00000346369.2:p.Ser352Thr
ENST00000358913.9:c.1879T>A	ENSP00000351790.5:p.Ser627Thr
ENST00000540630.5:c.1879T>A	ENSP00000441668.2:p.Ser627Thr
ENST00000613327.4:c.997T>A	ENSP00000480757.1:p.Ser333Thr
NM_001256267.1:c.1879T>A	NP_001243196.1:p.Ser627Thr
NM_001256268.1:c.997T>A	NP_001243197.1:p.Ser333Thr
NM_032578.3:c.1879T>A , LRG_410t1:c.1879T>A	NP_115967.2:p.Ser627Thr
NR_045662.3:n.1306T>A
NR_045663.3:n.2147T>A
XM_006718043.2:c.1933T>A	XP_006718106.1:p.Ser645Thr
XM_011540292.1:c.1909T>A	XP_011538594.1:p.Ser637Thr
XM_017016833.1:c.1957T>A	XP_016872322.1:p.Ser653Thr
XM_017016834.2:c.1879T>A	XP_016872323.1:p.Ser627Thr
XM_024448236.1:c.757T>A	XP_024304004.1:p.Ser253Thr
NR_045662.4:n.1416T>A
NR_045663.4:n.2092T>A
NM_001256267.2:c.1879T>A	NP_001243196.1:p.Ser627Thr
NM_001256268.2:c.997T>A	NP_001243197.1:p.Ser333Thr
NM_032578.4:c.1879T>A MANE Select	NP_115967.2:p.Ser627Thr