Canonical Allele Identifier: CA208195680

Gene: MYPN

Linked Data

• dbSNP Id: rs1028324916
• gnomAD v3: 10-68210548-G-GT
• gnomAD v4: 10-68210548-G-GT
• MyVariant Identifiers: chr10:g.69970305_69970306insT (hg19) ; chr10:g.68210548_68210549insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210549dup , CM000672.2:g.68210549dup	GRCh38
NC_000010.10:g.69970306dup , CM000672.1:g.69970306dup	GRCh37
NC_000010.9:g.69640312dup	NCBI36
NG_032118.1:g.109433dup , LRG_410:g.109433dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*94dup	ENSP00000346369.2:n.*94dup
ENST00000540630.6:c.*94dup	ENSP00000441668.3:n.*94dup
ENST00000613327.5:c.*94dup	ENSP00000480757.2:n.*94dup
ENST00000688812.1:c.*1320dup	ENSP00000510658.1:n.*1320dup
ENST00000690544.1:c.*3328dup	ENSP00000508989.1:n.*3328dup
ENST00000358913.10:c.*94dup MANE Select	ENSP00000351790.5:n.*94dup
ENST00000354393.6:c.*94dup	ENSP00000346369.2:n.*94dup
ENST00000358913.9:c.*94dup	ENSP00000351790.5:n.*94dup
ENST00000540630.5:c.*94dup	ENSP00000441668.2:n.*94dup
ENST00000613327.4:c.*94dup	ENSP00000480757.1:n.*94dup
NM_001256267.1:c.*94dup	NP_001243196.1:n.*94dup
NM_001256268.1:c.*94dup	NP_001243197.1:n.*94dup
NM_032578.3:c.*94dup , LRG_410t1:c.*94dup	NP_115967.2:n.*94dup
NR_045662.3:n.3484dup
NR_045663.3:n.4186dup
XM_006718043.2:c.*94dup	XP_006718106.1:n.*94dup
XM_011540292.1:c.*94dup	XP_011538594.1:n.*94dup
XR_946029.1:n.1574+4739dup
XM_017016833.1:c.*94dup	XP_016872322.1:n.*94dup
XM_017016834.2:c.*94dup	XP_016872323.1:n.*94dup
XM_024448236.1:c.*94dup	XP_024304004.1:n.*94dup
NR_045662.4:n.3594dup
NR_045663.4:n.4131dup
NM_001256267.2:c.*94dup	NP_001243196.1:n.*94dup
NM_001256268.2:c.*94dup	NP_001243197.1:n.*94dup
NM_032578.4:c.*94dup MANE Select	NP_115967.2:n.*94dup