Canonical Allele Identifier: CA376857439

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955240C>A (hg19) ; chr10:g.68195483C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195483C>A , CM000672.2:g.68195483C>A	GRCh38
NC_000010.10:g.69955240C>A , CM000672.1:g.69955240C>A	GRCh37
NC_000010.9:g.69625246C>A	NCBI36
NG_032118.1:g.94367C>A , LRG_410:g.94367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2284C>A	ENSP00000346369.2:p.Gln762Lys
ENST00000540630.6:c.3163C>A	ENSP00000441668.3:p.Gln1055Lys
ENST00000613327.5:c.3109C>A	ENSP00000480757.2:p.Gln1037Lys
ENST00000688812.1:c.*372C>A	ENSP00000510658.1:n.*372C>A
ENST00000690544.1:c.*2380C>A	ENSP00000508989.1:n.*2380C>A
ENST00000358913.10:c.3109C>A MANE Select	ENSP00000351790.5:p.Gln1037Lys
ENST00000354393.6:c.2284C>A	ENSP00000346369.2:p.Gln762Lys
ENST00000358913.9:c.3109C>A	ENSP00000351790.5:p.Gln1037Lys
ENST00000540630.5:c.3109C>A	ENSP00000441668.2:p.Gln1037Lys
ENST00000613327.4:c.2227C>A	ENSP00000480757.1:p.Gln743Lys
NM_001256267.1:c.3109C>A	NP_001243196.1:p.Gln1037Lys
NM_001256268.1:c.2227C>A	NP_001243197.1:p.Gln743Lys
NM_032578.3:c.3109C>A , LRG_410t1:c.3109C>A	NP_115967.2:p.Gln1037Lys
NR_045662.3:n.2536C>A
NR_045663.3:n.3238C>A
XM_006718043.2:c.3163C>A	XP_006718106.1:p.Gln1055Lys
XM_011540292.1:c.3139C>A	XP_011538594.1:p.Gln1047Lys
XM_017016833.1:c.3187C>A	XP_016872322.1:p.Gln1063Lys
XM_017016834.2:c.3109C>A	XP_016872323.1:p.Gln1037Lys
XM_024448236.1:c.1987C>A	XP_024304004.1:p.Gln663Lys
NR_045662.4:n.2646C>A
NR_045663.4:n.3183C>A
NM_001256267.2:c.3109C>A	NP_001243196.1:p.Gln1037Lys
NM_001256268.2:c.2227C>A	NP_001243197.1:p.Gln743Lys
NM_032578.4:c.3109C>A MANE Select	NP_115967.2:p.Gln1037Lys