Canonical Allele Identifier: CA376840389

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926281G>C (hg19) ; chr10:g.68166524G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166524G>C , CM000672.2:g.68166524G>C	GRCh38
NC_000010.10:g.69926281G>C , CM000672.1:g.69926281G>C	GRCh37
NC_000010.9:g.69596287G>C	NCBI36
NG_032118.1:g.65408G>C , LRG_410:g.65408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1006G>C	ENSP00000346369.2:p.Ala336Pro
ENST00000373675.4:c.1831G>C	ENSP00000362779.4:p.Ala611Pro
ENST00000540630.6:c.1885G>C	ENSP00000441668.3:p.Ala629Pro
ENST00000613327.5:c.1831G>C	ENSP00000480757.2:p.Ala611Pro
ENST00000687572.1:c.709G>C	ENSP00000510427.1:p.Ala237Pro
ENST00000688812.1:c.1807G>C	ENSP00000510658.1:p.Ala603Pro
ENST00000690544.1:c.*1102G>C	ENSP00000508989.1:n.*1102G>C
ENST00000358913.10:c.1831G>C MANE Select	ENSP00000351790.5:p.Ala611Pro
ENST00000354393.6:c.1006G>C	ENSP00000346369.2:p.Ala336Pro
ENST00000358913.9:c.1831G>C	ENSP00000351790.5:p.Ala611Pro
ENST00000540630.5:c.1831G>C	ENSP00000441668.2:p.Ala611Pro
ENST00000613327.4:c.949G>C	ENSP00000480757.1:p.Ala317Pro
NM_001256267.1:c.1831G>C	NP_001243196.1:p.Ala611Pro
NM_001256268.1:c.949G>C	NP_001243197.1:p.Ala317Pro
NM_032578.3:c.1831G>C , LRG_410t1:c.1831G>C	NP_115967.2:p.Ala611Pro
NR_045662.3:n.1258G>C
NR_045663.3:n.2099G>C
XM_006718043.2:c.1885G>C	XP_006718106.1:p.Ala629Pro
XM_011540292.1:c.1861G>C	XP_011538594.1:p.Ala621Pro
XM_017016833.1:c.1909G>C	XP_016872322.1:p.Ala637Pro
XM_017016834.2:c.1831G>C	XP_016872323.1:p.Ala611Pro
XM_024448236.1:c.709G>C	XP_024304004.1:p.Ala237Pro
NR_045662.4:n.1368G>C
NR_045663.4:n.2044G>C
NM_001256267.2:c.1831G>C	NP_001243196.1:p.Ala611Pro
NM_001256268.2:c.949G>C	NP_001243197.1:p.Ala317Pro
NM_032578.4:c.1831G>C MANE Select	NP_115967.2:p.Ala611Pro