Canonical Allele Identifier: CA376840636

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926337G>C (hg19) ; chr10:g.68166580G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166580G>C , CM000672.2:g.68166580G>C	GRCh38
NC_000010.10:g.69926337G>C , CM000672.1:g.69926337G>C	GRCh37
NC_000010.9:g.69596343G>C	NCBI36
NG_032118.1:g.65464G>C , LRG_410:g.65464G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1062G>C	ENSP00000346369.2:p.Gln354His
ENST00000373675.4:c.1887G>C	ENSP00000362779.4:p.Gln629His
ENST00000540630.6:c.1941G>C	ENSP00000441668.3:p.Gln647His
ENST00000613327.5:c.1887G>C	ENSP00000480757.2:p.Gln629His
ENST00000687572.1:c.765G>C	ENSP00000510427.1:p.Gln255His
ENST00000688812.1:c.1863G>C	ENSP00000510658.1:p.Gln621His
ENST00000690544.1:c.*1158G>C	ENSP00000508989.1:n.*1158G>C
ENST00000358913.10:c.1887G>C MANE Select	ENSP00000351790.5:p.Gln629His
ENST00000354393.6:c.1062G>C	ENSP00000346369.2:p.Gln354His
ENST00000358913.9:c.1887G>C	ENSP00000351790.5:p.Gln629His
ENST00000540630.5:c.1887G>C	ENSP00000441668.2:p.Gln629His
ENST00000613327.4:c.1005G>C	ENSP00000480757.1:p.Gln335His
NM_001256267.1:c.1887G>C	NP_001243196.1:p.Gln629His
NM_001256268.1:c.1005G>C	NP_001243197.1:p.Gln335His
NM_032578.3:c.1887G>C , LRG_410t1:c.1887G>C	NP_115967.2:p.Gln629His
NR_045662.3:n.1314G>C
NR_045663.3:n.2155G>C
XM_006718043.2:c.1941G>C	XP_006718106.1:p.Gln647His
XM_011540292.1:c.1917G>C	XP_011538594.1:p.Gln639His
XM_017016833.1:c.1965G>C	XP_016872322.1:p.Gln655His
XM_017016834.2:c.1887G>C	XP_016872323.1:p.Gln629His
XM_024448236.1:c.765G>C	XP_024304004.1:p.Gln255His
NR_045662.4:n.1424G>C
NR_045663.4:n.2100G>C
NM_001256267.2:c.1887G>C	NP_001243196.1:p.Gln629His
NM_001256268.2:c.1005G>C	NP_001243197.1:p.Gln335His
NM_032578.4:c.1887G>C MANE Select	NP_115967.2:p.Gln629His