Canonical Allele Identifier: CA469812123

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195455-A-G
• MyVariant Identifiers: chr10:g.69955212A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195455A>G , CM000672.2:g.68195455A>G	GRCh38
NC_000010.10:g.69955212A>G , CM000672.1:g.69955212A>G	GRCh37
NC_000010.9:g.69625218A>G	NCBI36
NG_032118.1:g.94339A>G , LRG_410:g.94339A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2256A>G	ENSP00000346369.2:p.Arg752=
ENST00000540630.6:c.3135A>G	ENSP00000441668.3:p.Arg1045=
ENST00000613327.5:c.3081A>G	ENSP00000480757.2:p.Arg1027=
ENST00000688812.1:c.*344A>G	ENSP00000510658.1:n.*344A>G
ENST00000690544.1:c.*2352A>G	ENSP00000508989.1:n.*2352A>G
ENST00000358913.10:c.3081A>G MANE Select	ENSP00000351790.5:p.Arg1027=
ENST00000354393.6:c.2256A>G	ENSP00000346369.2:p.Arg752=
ENST00000358913.9:c.3081A>G	ENSP00000351790.5:p.Arg1027=
ENST00000540630.5:c.3081A>G	ENSP00000441668.2:p.Arg1027=
ENST00000613327.4:c.2199A>G	ENSP00000480757.1:p.Arg733=
NM_001256267.1:c.3081A>G	NP_001243196.1:p.Arg1027=
NM_001256268.1:c.2199A>G	NP_001243197.1:p.Arg733=
NM_032578.3:c.3081A>G , LRG_410t1:c.3081A>G	NP_115967.2:p.Arg1027=
NR_045662.3:n.2508A>G
NR_045663.3:n.3210A>G
XM_006718043.2:c.3135A>G	XP_006718106.1:p.Arg1045=
XM_011540292.1:c.3111A>G	XP_011538594.1:p.Arg1037=
XM_017016833.1:c.3159A>G	XP_016872322.1:p.Arg1053=
XM_017016834.2:c.3081A>G	XP_016872323.1:p.Arg1027=
XM_024448236.1:c.1959A>G	XP_024304004.1:p.Arg653=
NR_045662.4:n.2618A>G
NR_045663.4:n.3155A>G
NM_001256267.2:c.3081A>G	NP_001243196.1:p.Arg1027=
NM_001256268.2:c.2199A>G	NP_001243197.1:p.Arg733=
NM_032578.4:c.3081A>G MANE Select	NP_115967.2:p.Arg1027=