Canonical Allele Identifier: CA469812219

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69957131A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197374A>C , CM000672.2:g.68197374A>C	GRCh38
NC_000010.10:g.69957131A>C , CM000672.1:g.69957131A>C	GRCh37
NC_000010.9:g.69627137A>C	NCBI36
NG_032118.1:g.96258A>C , LRG_410:g.96258A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2356A>C	ENSP00000346369.2:p.Arg786=
ENST00000540630.6:c.3235A>C	ENSP00000441668.3:p.Arg1079=
ENST00000613327.5:c.3181A>C	ENSP00000480757.2:p.Arg1061=
ENST00000688812.1:c.*444A>C	ENSP00000510658.1:n.*444A>C
ENST00000690544.1:c.*2452A>C	ENSP00000508989.1:n.*2452A>C
ENST00000358913.10:c.3181A>C MANE Select	ENSP00000351790.5:p.Arg1061=
ENST00000354393.6:c.2356A>C	ENSP00000346369.2:p.Arg786=
ENST00000358913.9:c.3181A>C	ENSP00000351790.5:p.Arg1061=
ENST00000540630.5:c.3181A>C	ENSP00000441668.2:p.Arg1061=
ENST00000613327.4:c.2299A>C	ENSP00000480757.1:p.Arg767=
NM_001256267.1:c.3181A>C	NP_001243196.1:p.Arg1061=
NM_001256268.1:c.2299A>C	NP_001243197.1:p.Arg767=
NM_032578.3:c.3181A>C , LRG_410t1:c.3181A>C	NP_115967.2:p.Arg1061=
NR_045662.3:n.2608A>C
NR_045663.3:n.3310A>C
XM_006718043.2:c.3235A>C	XP_006718106.1:p.Arg1079=
XM_011540292.1:c.3211A>C	XP_011538594.1:p.Arg1071=
XM_017016833.1:c.3259A>C	XP_016872322.1:p.Arg1087=
XM_017016834.2:c.3181A>C	XP_016872323.1:p.Arg1061=
XM_024448236.1:c.2059A>C	XP_024304004.1:p.Arg687=
NR_045662.4:n.2718A>C
NR_045663.4:n.3255A>C
NM_001256267.2:c.3181A>C	NP_001243196.1:p.Arg1061=
NM_001256268.2:c.2299A>C	NP_001243197.1:p.Arg767=
NM_032578.4:c.3181A>C MANE Select	NP_115967.2:p.Arg1061=