Canonical Allele Identifier: CA376857652

Gene: MYPN

Linked Data

• dbSNP Id: rs2043589867
• MyVariant Identifiers: chr10:g.69955271C>G (hg19) ; chr10:g.68195514C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195514C>G , CM000672.2:g.68195514C>G	GRCh38
NC_000010.10:g.69955271C>G , CM000672.1:g.69955271C>G	GRCh37
NC_000010.9:g.69625277C>G	NCBI36
NG_032118.1:g.94398C>G , LRG_410:g.94398C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2315C>G	ENSP00000346369.2:p.Ser772Cys
ENST00000540630.6:c.3194C>G	ENSP00000441668.3:p.Ser1065Cys
ENST00000613327.5:c.3140C>G	ENSP00000480757.2:p.Ser1047Cys
ENST00000688812.1:c.*403C>G	ENSP00000510658.1:n.*403C>G
ENST00000690544.1:c.*2411C>G	ENSP00000508989.1:n.*2411C>G
ENST00000358913.10:c.3140C>G MANE Select	ENSP00000351790.5:p.Ser1047Cys
ENST00000354393.6:c.2315C>G	ENSP00000346369.2:p.Ser772Cys
ENST00000358913.9:c.3140C>G	ENSP00000351790.5:p.Ser1047Cys
ENST00000540630.5:c.3140C>G	ENSP00000441668.2:p.Ser1047Cys
ENST00000613327.4:c.2258C>G	ENSP00000480757.1:p.Ser753Cys
NM_001256267.1:c.3140C>G	NP_001243196.1:p.Ser1047Cys
NM_001256268.1:c.2258C>G	NP_001243197.1:p.Ser753Cys
NM_032578.3:c.3140C>G , LRG_410t1:c.3140C>G	NP_115967.2:p.Ser1047Cys
NR_045662.3:n.2567C>G
NR_045663.3:n.3269C>G
XM_006718043.2:c.3194C>G	XP_006718106.1:p.Ser1065Cys
XM_011540292.1:c.3170C>G	XP_011538594.1:p.Ser1057Cys
XM_017016833.1:c.3218C>G	XP_016872322.1:p.Ser1073Cys
XM_017016834.2:c.3140C>G	XP_016872323.1:p.Ser1047Cys
XM_024448236.1:c.2018C>G	XP_024304004.1:p.Ser673Cys
NR_045662.4:n.2677C>G
NR_045663.4:n.3214C>G
NM_001256267.2:c.3140C>G	NP_001243196.1:p.Ser1047Cys
NM_001256268.2:c.2258C>G	NP_001243197.1:p.Ser753Cys
NM_032578.4:c.3140C>G MANE Select	NP_115967.2:p.Ser1047Cys