Canonical Allele Identifier: CA376830080

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69970119A>C (hg19) ; chr10:g.68210362A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210362A>C , CM000672.2:g.68210362A>C	GRCh38
NC_000010.10:g.69970119A>C , CM000672.1:g.69970119A>C	GRCh37
NC_000010.9:g.69640125A>C	NCBI36
NG_032118.1:g.109246A>C , LRG_410:g.109246A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.3045A>C	ENSP00000346369.2:p.Lys1015Asn
ENST00000540630.6:c.3924A>C	ENSP00000441668.3:p.Lys1308Asn
ENST00000613327.5:c.3870A>C	ENSP00000480757.2:p.Lys1290Asn
ENST00000688812.1:c.*1133A>C	ENSP00000510658.1:n.*1133A>C
ENST00000690544.1:c.*3141A>C	ENSP00000508989.1:n.*3141A>C
ENST00000358913.10:c.3870A>C MANE Select	ENSP00000351790.5:p.Lys1290Asn
ENST00000354393.6:c.3045A>C	ENSP00000346369.2:p.Lys1015Asn
ENST00000358913.9:c.3870A>C	ENSP00000351790.5:p.Lys1290Asn
ENST00000540630.5:c.3870A>C	ENSP00000441668.2:p.Lys1290Asn
ENST00000613327.4:c.2988A>C	ENSP00000480757.1:p.Lys996Asn
NM_001256267.1:c.3870A>C	NP_001243196.1:p.Lys1290Asn
NM_001256268.1:c.2988A>C	NP_001243197.1:p.Lys996Asn
NM_032578.3:c.3870A>C , LRG_410t1:c.3870A>C	NP_115967.2:p.Lys1290Asn
NR_045662.3:n.3297A>C
NR_045663.3:n.3999A>C
XM_006718043.2:c.3924A>C	XP_006718106.1:p.Lys1308Asn
XM_011540292.1:c.3900A>C	XP_011538594.1:p.Lys1300Asn
XR_946029.1:n.1574+4926T>G
XM_017016833.1:c.3948A>C	XP_016872322.1:p.Lys1316Asn
XM_017016834.2:c.3870A>C	XP_016872323.1:p.Lys1290Asn
XM_024448236.1:c.2748A>C	XP_024304004.1:p.Lys916Asn
NR_045662.4:n.3407A>C
NR_045663.4:n.3944A>C
NM_001256267.2:c.3870A>C	NP_001243196.1:p.Lys1290Asn
NM_001256268.2:c.2988A>C	NP_001243197.1:p.Lys996Asn
NM_032578.4:c.3870A>C MANE Select	NP_115967.2:p.Lys1290Asn