Canonical Allele Identifier: CA376840431

Gene: MYPN

Linked Data

• ClinVar Variation Id: 3228157
• ClinVar RCV Id: RCV004519867
• MyVariant Identifiers: chr10:g.69926293G>A (hg19) ; chr10:g.68166536G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166536G>A , CM000672.2:g.68166536G>A	GRCh38
NC_000010.10:g.69926293G>A , CM000672.1:g.69926293G>A	GRCh37
NC_000010.9:g.69596299G>A	NCBI36
NG_032118.1:g.65420G>A , LRG_410:g.65420G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1018G>A	ENSP00000346369.2:p.Ala340Thr
ENST00000373675.4:c.1843G>A	ENSP00000362779.4:p.Ala615Thr
ENST00000540630.6:c.1897G>A	ENSP00000441668.3:p.Ala633Thr
ENST00000613327.5:c.1843G>A	ENSP00000480757.2:p.Ala615Thr
ENST00000687572.1:c.721G>A	ENSP00000510427.1:p.Ala241Thr
ENST00000688812.1:c.1819G>A	ENSP00000510658.1:p.Ala607Thr
ENST00000690544.1:c.*1114G>A	ENSP00000508989.1:n.*1114G>A
ENST00000358913.10:c.1843G>A MANE Select	ENSP00000351790.5:p.Ala615Thr
ENST00000354393.6:c.1018G>A	ENSP00000346369.2:p.Ala340Thr
ENST00000358913.9:c.1843G>A	ENSP00000351790.5:p.Ala615Thr
ENST00000540630.5:c.1843G>A	ENSP00000441668.2:p.Ala615Thr
ENST00000613327.4:c.961G>A	ENSP00000480757.1:p.Ala321Thr
NM_001256267.1:c.1843G>A	NP_001243196.1:p.Ala615Thr
NM_001256268.1:c.961G>A	NP_001243197.1:p.Ala321Thr
NM_032578.3:c.1843G>A , LRG_410t1:c.1843G>A	NP_115967.2:p.Ala615Thr
NR_045662.3:n.1270G>A
NR_045663.3:n.2111G>A
XM_006718043.2:c.1897G>A	XP_006718106.1:p.Ala633Thr
XM_011540292.1:c.1873G>A	XP_011538594.1:p.Ala625Thr
XM_017016833.1:c.1921G>A	XP_016872322.1:p.Ala641Thr
XM_017016834.2:c.1843G>A	XP_016872323.1:p.Ala615Thr
XM_024448236.1:c.721G>A	XP_024304004.1:p.Ala241Thr
NR_045662.4:n.1380G>A
NR_045663.4:n.2056G>A
NM_001256267.2:c.1843G>A	NP_001243196.1:p.Ala615Thr
NM_001256268.2:c.961G>A	NP_001243197.1:p.Ala321Thr
NM_032578.4:c.1843G>A MANE Select	NP_115967.2:p.Ala615Thr