Canonical Allele Identifier: CA376839361

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926071A>C (hg19) ; chr10:g.68166314A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166314A>C , CM000672.2:g.68166314A>C	GRCh38
NC_000010.10:g.69926071A>C , CM000672.1:g.69926071A>C	GRCh37
NC_000010.9:g.69596077A>C	NCBI36
NG_032118.1:g.65198A>C , LRG_410:g.65198A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.796A>C	ENSP00000346369.2:p.Asn266His
ENST00000373675.4:c.1621A>C	ENSP00000362779.4:p.Asn541His
ENST00000540630.6:c.1675A>C	ENSP00000441668.3:p.Asn559His
ENST00000613327.5:c.1621A>C	ENSP00000480757.2:p.Asn541His
ENST00000687572.1:c.499A>C	ENSP00000510427.1:p.Asn167His
ENST00000687705.1:c.*1870A>C	ENSP00000509639.1:n.*1870A>C
ENST00000688812.1:c.1597A>C	ENSP00000510658.1:p.Asn533His
ENST00000689002.1:n.673A>C
ENST00000690544.1:c.*892A>C	ENSP00000508989.1:n.*892A>C
ENST00000358913.10:c.1621A>C MANE Select	ENSP00000351790.5:p.Asn541His
ENST00000354393.6:c.796A>C	ENSP00000346369.2:p.Asn266His
ENST00000358913.9:c.1621A>C	ENSP00000351790.5:p.Asn541His
ENST00000540630.5:c.1621A>C	ENSP00000441668.2:p.Asn541His
ENST00000613327.4:c.739A>C	ENSP00000480757.1:p.Asn247His
NM_001256267.1:c.1621A>C	NP_001243196.1:p.Asn541His
NM_001256268.1:c.739A>C	NP_001243197.1:p.Asn247His
NM_032578.3:c.1621A>C , LRG_410t1:c.1621A>C	NP_115967.2:p.Asn541His
NR_045662.3:n.1048A>C
NR_045663.3:n.1889A>C
XM_006718043.2:c.1675A>C	XP_006718106.1:p.Asn559His
XM_011540292.1:c.1651A>C	XP_011538594.1:p.Asn551His
XM_017016833.1:c.1699A>C	XP_016872322.1:p.Asn567His
XM_017016834.2:c.1621A>C	XP_016872323.1:p.Asn541His
XM_024448236.1:c.499A>C	XP_024304004.1:p.Asn167His
NR_045662.4:n.1158A>C
NR_045663.4:n.1834A>C
NM_001256267.2:c.1621A>C	NP_001243196.1:p.Asn541His
NM_001256268.2:c.739A>C	NP_001243197.1:p.Asn247His
NM_032578.4:c.1621A>C MANE Select	NP_115967.2:p.Asn541His