Canonical Allele Identifier: CA469812164

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955263G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195506G>C , CM000672.2:g.68195506G>C	GRCh38
NC_000010.10:g.69955263G>C , CM000672.1:g.69955263G>C	GRCh37
NC_000010.9:g.69625269G>C	NCBI36
NG_032118.1:g.94390G>C , LRG_410:g.94390G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2307G>C	ENSP00000346369.2:p.Arg769=
ENST00000540630.6:c.3186G>C	ENSP00000441668.3:p.Arg1062=
ENST00000613327.5:c.3132G>C	ENSP00000480757.2:p.Arg1044=
ENST00000688812.1:c.*395G>C	ENSP00000510658.1:n.*395G>C
ENST00000690544.1:c.*2403G>C	ENSP00000508989.1:n.*2403G>C
ENST00000358913.10:c.3132G>C MANE Select	ENSP00000351790.5:p.Arg1044=
ENST00000354393.6:c.2307G>C	ENSP00000346369.2:p.Arg769=
ENST00000358913.9:c.3132G>C	ENSP00000351790.5:p.Arg1044=
ENST00000540630.5:c.3132G>C	ENSP00000441668.2:p.Arg1044=
ENST00000613327.4:c.2250G>C	ENSP00000480757.1:p.Arg750=
NM_001256267.1:c.3132G>C	NP_001243196.1:p.Arg1044=
NM_001256268.1:c.2250G>C	NP_001243197.1:p.Arg750=
NM_032578.3:c.3132G>C , LRG_410t1:c.3132G>C	NP_115967.2:p.Arg1044=
NR_045662.3:n.2559G>C
NR_045663.3:n.3261G>C
XM_006718043.2:c.3186G>C	XP_006718106.1:p.Arg1062=
XM_011540292.1:c.3162G>C	XP_011538594.1:p.Arg1054=
XM_017016833.1:c.3210G>C	XP_016872322.1:p.Arg1070=
XM_017016834.2:c.3132G>C	XP_016872323.1:p.Arg1044=
XM_024448236.1:c.2010G>C	XP_024304004.1:p.Arg670=
NR_045662.4:n.2669G>C
NR_045663.4:n.3206G>C
NM_001256267.2:c.3132G>C	NP_001243196.1:p.Arg1044=
NM_001256268.2:c.2250G>C	NP_001243197.1:p.Arg750=
NM_032578.4:c.3132G>C MANE Select	NP_115967.2:p.Arg1044=