Canonical Allele Identifier: CA376829913

Gene: MYPN

Linked Data

• dbSNP Id: rs370197106
• gnomAD v2: 10-69970073-T-A
• gnomAD v4: 10-68210316-T-A
• MyVariant Identifiers: chr10:g.69970073T>A (hg19) ; chr10:g.68210316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210316T>A , CM000672.2:g.68210316T>A	GRCh38
NC_000010.10:g.69970073T>A , CM000672.1:g.69970073T>A	GRCh37
NC_000010.9:g.69640079T>A	NCBI36
NG_032118.1:g.109200T>A , LRG_410:g.109200T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2999T>A	ENSP00000346369.2:p.Met1000Lys
ENST00000540630.6:c.3878T>A	ENSP00000441668.3:p.Met1293Lys
ENST00000613327.5:c.3824T>A	ENSP00000480757.2:p.Met1275Lys
ENST00000688812.1:c.*1087T>A	ENSP00000510658.1:n.*1087T>A
ENST00000690544.1:c.*3095T>A	ENSP00000508989.1:n.*3095T>A
ENST00000358913.10:c.3824T>A MANE Select	ENSP00000351790.5:p.Met1275Lys
ENST00000354393.6:c.2999T>A	ENSP00000346369.2:p.Met1000Lys
ENST00000358913.9:c.3824T>A	ENSP00000351790.5:p.Met1275Lys
ENST00000540630.5:c.3824T>A	ENSP00000441668.2:p.Met1275Lys
ENST00000613327.4:c.2942T>A	ENSP00000480757.1:p.Met981Lys
NM_001256267.1:c.3824T>A	NP_001243196.1:p.Met1275Lys
NM_001256268.1:c.2942T>A	NP_001243197.1:p.Met981Lys
NM_032578.3:c.3824T>A , LRG_410t1:c.3824T>A	NP_115967.2:p.Met1275Lys
NR_045662.3:n.3251T>A
NR_045663.3:n.3953T>A
XM_006718043.2:c.3878T>A	XP_006718106.1:p.Met1293Lys
XM_011540292.1:c.3854T>A	XP_011538594.1:p.Met1285Lys
XR_946029.1:n.1574+4972A>T
XM_017016833.1:c.3902T>A	XP_016872322.1:p.Met1301Lys
XM_017016834.2:c.3824T>A	XP_016872323.1:p.Met1275Lys
XM_024448236.1:c.2702T>A	XP_024304004.1:p.Met901Lys
NR_045662.4:n.3361T>A
NR_045663.4:n.3898T>A
NM_001256267.2:c.3824T>A	NP_001243196.1:p.Met1275Lys
NM_001256268.2:c.2942T>A	NP_001243197.1:p.Met981Lys
NM_032578.4:c.3824T>A MANE Select	NP_115967.2:p.Met1275Lys