Canonical Allele Identifier: CA5522665

Gene: MYPN

Linked Data

• dbSNP Id: rs747946013
• ExAC: 10:69926276 G / A
• gnomAD v2: 10-69926276-G-A
• gnomAD v4: 10-68166519-G-A
• MyVariant Identifiers: chr10:g.69926276G>A (hg19) ; chr10:g.68166519G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166519G>A , CM000672.2:g.68166519G>A	GRCh38
NC_000010.10:g.69926276G>A , CM000672.1:g.69926276G>A	GRCh37
NC_000010.9:g.69596282G>A	NCBI36
NG_032118.1:g.65403G>A , LRG_410:g.65403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1001G>A	ENSP00000346369.2:p.Ser334Asn
ENST00000373675.4:c.1826G>A	ENSP00000362779.4:p.Ser609Asn
ENST00000540630.6:c.1880G>A	ENSP00000441668.3:p.Ser627Asn
ENST00000613327.5:c.1826G>A	ENSP00000480757.2:p.Ser609Asn
ENST00000687572.1:c.704G>A	ENSP00000510427.1:p.Ser235Asn
ENST00000688812.1:c.1802G>A	ENSP00000510658.1:p.Ser601Asn
ENST00000690544.1:c.*1097G>A	ENSP00000508989.1:n.*1097G>A
ENST00000358913.10:c.1826G>A MANE Select	ENSP00000351790.5:p.Ser609Asn
ENST00000354393.6:c.1001G>A	ENSP00000346369.2:p.Ser334Asn
ENST00000358913.9:c.1826G>A	ENSP00000351790.5:p.Ser609Asn
ENST00000540630.5:c.1826G>A	ENSP00000441668.2:p.Ser609Asn
ENST00000613327.4:c.944G>A	ENSP00000480757.1:p.Ser315Asn
NM_001256267.1:c.1826G>A	NP_001243196.1:p.Ser609Asn
NM_001256268.1:c.944G>A	NP_001243197.1:p.Ser315Asn
NM_032578.3:c.1826G>A , LRG_410t1:c.1826G>A	NP_115967.2:p.Ser609Asn
NR_045662.3:n.1253G>A
NR_045663.3:n.2094G>A
XM_006718043.2:c.1880G>A	XP_006718106.1:p.Ser627Asn
XM_011540292.1:c.1856G>A	XP_011538594.1:p.Ser619Asn
XM_017016833.1:c.1904G>A	XP_016872322.1:p.Ser635Asn
XM_017016834.2:c.1826G>A	XP_016872323.1:p.Ser609Asn
XM_024448236.1:c.704G>A	XP_024304004.1:p.Ser235Asn
NR_045662.4:n.1363G>A
NR_045663.4:n.2039G>A
NM_001256267.2:c.1826G>A	NP_001243196.1:p.Ser609Asn
NM_001256268.2:c.944G>A	NP_001243197.1:p.Ser315Asn
NM_032578.4:c.1826G>A MANE Select	NP_115967.2:p.Ser609Asn