Canonical Allele Identifier: CA376859275

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199497-C-A
• MyVariant Identifiers: chr10:g.69959254C>A (hg19) ; chr10:g.68199497C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199497C>A , CM000672.2:g.68199497C>A	GRCh38
NC_000010.10:g.69959254C>A , CM000672.1:g.69959254C>A	GRCh37
NC_000010.9:g.69629260C>A	NCBI36
NG_032118.1:g.98381C>A , LRG_410:g.98381C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2590C>A	ENSP00000346369.2:p.Arg864Ser
ENST00000540630.6:c.3469C>A	ENSP00000441668.3:p.Arg1157Ser
ENST00000613327.5:c.3415C>A	ENSP00000480757.2:p.Arg1139Ser
ENST00000688812.1:c.*678C>A	ENSP00000510658.1:n.*678C>A
ENST00000690544.1:c.*2686C>A	ENSP00000508989.1:n.*2686C>A
ENST00000358913.10:c.3415C>A MANE Select	ENSP00000351790.5:p.Arg1139Ser
ENST00000354393.6:c.2590C>A	ENSP00000346369.2:p.Arg864Ser
ENST00000358913.9:c.3415C>A	ENSP00000351790.5:p.Arg1139Ser
ENST00000540630.5:c.3415C>A	ENSP00000441668.2:p.Arg1139Ser
ENST00000613327.4:c.2533C>A	ENSP00000480757.1:p.Arg845Ser
NM_001256267.1:c.3415C>A	NP_001243196.1:p.Arg1139Ser
NM_001256268.1:c.2533C>A	NP_001243197.1:p.Arg845Ser
NM_032578.3:c.3415C>A , LRG_410t1:c.3415C>A	NP_115967.2:p.Arg1139Ser
NR_045662.3:n.2842C>A
NR_045663.3:n.3544C>A
XM_006718043.2:c.3469C>A	XP_006718106.1:p.Arg1157Ser
XM_011540292.1:c.3445C>A	XP_011538594.1:p.Arg1149Ser
XR_946029.1:n.1804-222G>T
XM_017016833.1:c.3493C>A	XP_016872322.1:p.Arg1165Ser
XM_017016834.2:c.3415C>A	XP_016872323.1:p.Arg1139Ser
XM_024448236.1:c.2293C>A	XP_024304004.1:p.Arg765Ser
NR_045662.4:n.2952C>A
NR_045663.4:n.3489C>A
NM_001256267.2:c.3415C>A	NP_001243196.1:p.Arg1139Ser
NM_001256268.2:c.2533C>A	NP_001243197.1:p.Arg845Ser
NM_032578.4:c.3415C>A MANE Select	NP_115967.2:p.Arg1139Ser