Canonical Allele Identifier: CA376858864

Gene: MYPN

Linked Data

• dbSNP Id: rs1286901592
• gnomAD v2: 10-69959129-G-A
• gnomAD v4: 10-68199372-G-A
• MyVariant Identifiers: chr10:g.69959129G>A (hg19) ; chr10:g.68199372G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199372G>A , CM000672.2:g.68199372G>A	GRCh38
NC_000010.10:g.69959129G>A , CM000672.1:g.69959129G>A	GRCh37
NC_000010.9:g.69629135G>A	NCBI36
NG_032118.1:g.98256G>A , LRG_410:g.98256G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2465G>A	ENSP00000346369.2:p.Ser822Asn
ENST00000540630.6:c.3344G>A	ENSP00000441668.3:p.Ser1115Asn
ENST00000613327.5:c.3290G>A	ENSP00000480757.2:p.Ser1097Asn
ENST00000688812.1:c.*553G>A	ENSP00000510658.1:n.*553G>A
ENST00000690544.1:c.*2561G>A	ENSP00000508989.1:n.*2561G>A
ENST00000358913.10:c.3290G>A MANE Select	ENSP00000351790.5:p.Ser1097Asn
ENST00000354393.6:c.2465G>A	ENSP00000346369.2:p.Ser822Asn
ENST00000358913.9:c.3290G>A	ENSP00000351790.5:p.Ser1097Asn
ENST00000540630.5:c.3290G>A	ENSP00000441668.2:p.Ser1097Asn
ENST00000613327.4:c.2408G>A	ENSP00000480757.1:p.Ser803Asn
NM_001256267.1:c.3290G>A	NP_001243196.1:p.Ser1097Asn
NM_001256268.1:c.2408G>A	NP_001243197.1:p.Ser803Asn
NM_032578.3:c.3290G>A , LRG_410t1:c.3290G>A	NP_115967.2:p.Ser1097Asn
NR_045662.3:n.2717G>A
NR_045663.3:n.3419G>A
XM_006718043.2:c.3344G>A	XP_006718106.1:p.Ser1115Asn
XM_011540292.1:c.3320G>A	XP_011538594.1:p.Ser1107Asn
XR_946029.1:n.1804-97C>T
XM_017016833.1:c.3368G>A	XP_016872322.1:p.Ser1123Asn
XM_017016834.2:c.3290G>A	XP_016872323.1:p.Ser1097Asn
XM_024448236.1:c.2168G>A	XP_024304004.1:p.Ser723Asn
NR_045662.4:n.2827G>A
NR_045663.4:n.3364G>A
NM_001256267.2:c.3290G>A	NP_001243196.1:p.Ser1097Asn
NM_001256268.2:c.2408G>A	NP_001243197.1:p.Ser803Asn
NM_032578.4:c.3290G>A MANE Select	NP_115967.2:p.Ser1097Asn