Canonical Allele Identifier: CA376857649

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195514-C-A
• MyVariant Identifiers: chr10:g.69955271C>A (hg19) ; chr10:g.68195514C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2315C>A	ENSP00000346369.2:p.Ser772Tyr
ENST00000540630.6:c.3194C>A	ENSP00000441668.3:p.Ser1065Tyr
ENST00000613327.5:c.3140C>A	ENSP00000480757.2:p.Ser1047Tyr
ENST00000688812.1:c.*403C>A	ENSP00000510658.1:n.*403C>A
ENST00000690544.1:c.*2411C>A	ENSP00000508989.1:n.*2411C>A
ENST00000358913.10:c.3140C>A MANE Select	ENSP00000351790.5:p.Ser1047Tyr
ENST00000354393.6:c.2315C>A	ENSP00000346369.2:p.Ser772Tyr
ENST00000358913.9:c.3140C>A	ENSP00000351790.5:p.Ser1047Tyr
ENST00000540630.5:c.3140C>A	ENSP00000441668.2:p.Ser1047Tyr
ENST00000613327.4:c.2258C>A	ENSP00000480757.1:p.Ser753Tyr
NM_001256267.1:c.3140C>A	NP_001243196.1:p.Ser1047Tyr
NM_001256268.1:c.2258C>A	NP_001243197.1:p.Ser753Tyr
NM_032578.3:c.3140C>A , LRG_410t1:c.3140C>A	NP_115967.2:p.Ser1047Tyr
NR_045662.3:n.2567C>A
NR_045663.3:n.3269C>A
XM_006718043.2:c.3194C>A	XP_006718106.1:p.Ser1065Tyr
XM_011540292.1:c.3170C>A	XP_011538594.1:p.Ser1057Tyr
XM_017016833.1:c.3218C>A	XP_016872322.1:p.Ser1073Tyr
XM_017016834.2:c.3140C>A	XP_016872323.1:p.Ser1047Tyr
XM_024448236.1:c.2018C>A	XP_024304004.1:p.Ser673Tyr
NR_045662.4:n.2677C>A
NR_045663.4:n.3214C>A
NM_001256267.2:c.3140C>A	NP_001243196.1:p.Ser1047Tyr
NM_001256268.2:c.2258C>A	NP_001243197.1:p.Ser753Tyr
NM_032578.4:c.3140C>A MANE Select	NP_115967.2:p.Ser1047Tyr