Canonical Allele Identifier: CA469813035

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926370A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166613A>C , CM000672.2:g.68166613A>C	GRCh38
NC_000010.10:g.69926370A>C , CM000672.1:g.69926370A>C	GRCh37
NC_000010.9:g.69596376A>C	NCBI36
NG_032118.1:g.65497A>C , LRG_410:g.65497A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1095A>C	ENSP00000346369.2:p.Pro365=
ENST00000373675.4:c.1920A>C	ENSP00000362779.4:p.Pro640=
ENST00000540630.6:c.1974A>C	ENSP00000441668.3:p.Pro658=
ENST00000613327.5:c.1920A>C	ENSP00000480757.2:p.Pro640=
ENST00000687572.1:c.798A>C	ENSP00000510427.1:p.Pro266=
ENST00000688812.1:c.1896A>C	ENSP00000510658.1:p.Pro632=
ENST00000690544.1:c.*1191A>C	ENSP00000508989.1:n.*1191A>C
ENST00000358913.10:c.1920A>C MANE Select	ENSP00000351790.5:p.Pro640=
ENST00000354393.6:c.1095A>C	ENSP00000346369.2:p.Pro365=
ENST00000358913.9:c.1920A>C	ENSP00000351790.5:p.Pro640=
ENST00000540630.5:c.1920A>C	ENSP00000441668.2:p.Pro640=
ENST00000613327.4:c.1038A>C	ENSP00000480757.1:p.Pro346=
NM_001256267.1:c.1920A>C	NP_001243196.1:p.Pro640=
NM_001256268.1:c.1038A>C	NP_001243197.1:p.Pro346=
NM_032578.3:c.1920A>C , LRG_410t1:c.1920A>C	NP_115967.2:p.Pro640=
NR_045662.3:n.1347A>C
NR_045663.3:n.2188A>C
XM_006718043.2:c.1974A>C	XP_006718106.1:p.Pro658=
XM_011540292.1:c.1950A>C	XP_011538594.1:p.Pro650=
XM_017016833.1:c.1998A>C	XP_016872322.1:p.Pro666=
XM_017016834.2:c.1920A>C	XP_016872323.1:p.Pro640=
XM_024448236.1:c.798A>C	XP_024304004.1:p.Pro266=
NR_045662.4:n.1457A>C
NR_045663.4:n.2133A>C
NM_001256267.2:c.1920A>C	NP_001243196.1:p.Pro640=
NM_001256268.2:c.1038A>C	NP_001243197.1:p.Pro346=
NM_032578.4:c.1920A>C MANE Select	NP_115967.2:p.Pro640=