Canonical Allele Identifier: CA376840632

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926336A>C (hg19) ; chr10:g.68166579A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166579A>C , CM000672.2:g.68166579A>C	GRCh38
NC_000010.10:g.69926336A>C , CM000672.1:g.69926336A>C	GRCh37
NC_000010.9:g.69596342A>C	NCBI36
NG_032118.1:g.65463A>C , LRG_410:g.65463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1061A>C	ENSP00000346369.2:p.Gln354Pro
ENST00000373675.4:c.1886A>C	ENSP00000362779.4:p.Gln629Pro
ENST00000540630.6:c.1940A>C	ENSP00000441668.3:p.Gln647Pro
ENST00000613327.5:c.1886A>C	ENSP00000480757.2:p.Gln629Pro
ENST00000687572.1:c.764A>C	ENSP00000510427.1:p.Gln255Pro
ENST00000688812.1:c.1862A>C	ENSP00000510658.1:p.Gln621Pro
ENST00000690544.1:c.*1157A>C	ENSP00000508989.1:n.*1157A>C
ENST00000358913.10:c.1886A>C MANE Select	ENSP00000351790.5:p.Gln629Pro
ENST00000354393.6:c.1061A>C	ENSP00000346369.2:p.Gln354Pro
ENST00000358913.9:c.1886A>C	ENSP00000351790.5:p.Gln629Pro
ENST00000540630.5:c.1886A>C	ENSP00000441668.2:p.Gln629Pro
ENST00000613327.4:c.1004A>C	ENSP00000480757.1:p.Gln335Pro
NM_001256267.1:c.1886A>C	NP_001243196.1:p.Gln629Pro
NM_001256268.1:c.1004A>C	NP_001243197.1:p.Gln335Pro
NM_032578.3:c.1886A>C , LRG_410t1:c.1886A>C	NP_115967.2:p.Gln629Pro
NR_045662.3:n.1313A>C
NR_045663.3:n.2154A>C
XM_006718043.2:c.1940A>C	XP_006718106.1:p.Gln647Pro
XM_011540292.1:c.1916A>C	XP_011538594.1:p.Gln639Pro
XM_017016833.1:c.1964A>C	XP_016872322.1:p.Gln655Pro
XM_017016834.2:c.1886A>C	XP_016872323.1:p.Gln629Pro
XM_024448236.1:c.764A>C	XP_024304004.1:p.Gln255Pro
NR_045662.4:n.1423A>C
NR_045663.4:n.2099A>C
NM_001256267.2:c.1886A>C	NP_001243196.1:p.Gln629Pro
NM_001256268.2:c.1004A>C	NP_001243197.1:p.Gln335Pro
NM_032578.4:c.1886A>C MANE Select	NP_115967.2:p.Gln629Pro