Canonical Allele Identifier: CA469812174

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955272T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195515T>C , CM000672.2:g.68195515T>C	GRCh38
NC_000010.10:g.69955272T>C , CM000672.1:g.69955272T>C	GRCh37
NC_000010.9:g.69625278T>C	NCBI36
NG_032118.1:g.94399T>C , LRG_410:g.94399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2316T>C	ENSP00000346369.2:p.Ser772=
ENST00000540630.6:c.3195T>C	ENSP00000441668.3:p.Ser1065=
ENST00000613327.5:c.3141T>C	ENSP00000480757.2:p.Ser1047=
ENST00000688812.1:c.*404T>C	ENSP00000510658.1:n.*404T>C
ENST00000690544.1:c.*2412T>C	ENSP00000508989.1:n.*2412T>C
ENST00000358913.10:c.3141T>C MANE Select	ENSP00000351790.5:p.Ser1047=
ENST00000354393.6:c.2316T>C	ENSP00000346369.2:p.Ser772=
ENST00000358913.9:c.3141T>C	ENSP00000351790.5:p.Ser1047=
ENST00000540630.5:c.3141T>C	ENSP00000441668.2:p.Ser1047=
ENST00000613327.4:c.2259T>C	ENSP00000480757.1:p.Ser753=
NM_001256267.1:c.3141T>C	NP_001243196.1:p.Ser1047=
NM_001256268.1:c.2259T>C	NP_001243197.1:p.Ser753=
NM_032578.3:c.3141T>C , LRG_410t1:c.3141T>C	NP_115967.2:p.Ser1047=
NR_045662.3:n.2568T>C
NR_045663.3:n.3270T>C
XM_006718043.2:c.3195T>C	XP_006718106.1:p.Ser1065=
XM_011540292.1:c.3171T>C	XP_011538594.1:p.Ser1057=
XM_017016833.1:c.3219T>C	XP_016872322.1:p.Ser1073=
XM_017016834.2:c.3141T>C	XP_016872323.1:p.Ser1047=
XM_024448236.1:c.2019T>C	XP_024304004.1:p.Ser673=
NR_045662.4:n.2678T>C
NR_045663.4:n.3215T>C
NM_001256267.2:c.3141T>C	NP_001243196.1:p.Ser1047=
NM_001256268.2:c.2259T>C	NP_001243197.1:p.Ser753=
NM_032578.4:c.3141T>C MANE Select	NP_115967.2:p.Ser1047=