Canonical Allele Identifier: CA376841122

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926414A>C (hg19) ; chr10:g.68166657A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166657A>C , CM000672.2:g.68166657A>C	GRCh38
NC_000010.10:g.69926414A>C , CM000672.1:g.69926414A>C	GRCh37
NC_000010.9:g.69596420A>C	NCBI36
NG_032118.1:g.65541A>C , LRG_410:g.65541A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1139A>C	ENSP00000346369.2:p.Lys380Thr
ENST00000373675.4:c.1964A>C	ENSP00000362779.4:p.Lys655Thr
ENST00000540630.6:c.2018A>C	ENSP00000441668.3:p.Lys673Thr
ENST00000613327.5:c.1964A>C	ENSP00000480757.2:p.Lys655Thr
ENST00000687572.1:c.842A>C	ENSP00000510427.1:p.Lys281Thr
ENST00000688812.1:c.1940A>C	ENSP00000510658.1:p.Lys647Thr
ENST00000690544.1:c.*1235A>C	ENSP00000508989.1:n.*1235A>C
ENST00000358913.10:c.1964A>C MANE Select	ENSP00000351790.5:p.Lys655Thr
ENST00000354393.6:c.1139A>C	ENSP00000346369.2:p.Lys380Thr
ENST00000358913.9:c.1964A>C	ENSP00000351790.5:p.Lys655Thr
ENST00000540630.5:c.1964A>C	ENSP00000441668.2:p.Lys655Thr
ENST00000613327.4:c.1082A>C	ENSP00000480757.1:p.Lys361Thr
NM_001256267.1:c.1964A>C	NP_001243196.1:p.Lys655Thr
NM_001256268.1:c.1082A>C	NP_001243197.1:p.Lys361Thr
NM_032578.3:c.1964A>C , LRG_410t1:c.1964A>C	NP_115967.2:p.Lys655Thr
NR_045662.3:n.1391A>C
NR_045663.3:n.2232A>C
XM_006718043.2:c.2018A>C	XP_006718106.1:p.Lys673Thr
XM_011540292.1:c.1994A>C	XP_011538594.1:p.Lys665Thr
XM_017016833.1:c.2042A>C	XP_016872322.1:p.Lys681Thr
XM_017016834.2:c.1964A>C	XP_016872323.1:p.Lys655Thr
XM_024448236.1:c.842A>C	XP_024304004.1:p.Lys281Thr
NR_045662.4:n.1501A>C
NR_045663.4:n.2177A>C
NM_001256267.2:c.1964A>C	NP_001243196.1:p.Lys655Thr
NM_001256268.2:c.1082A>C	NP_001243197.1:p.Lys361Thr
NM_032578.4:c.1964A>C MANE Select	NP_115967.2:p.Lys655Thr