Canonical Allele Identifier: CA593803335

Gene: MYPN

Linked Data

• dbSNP Id: rs1491122542
• gnomAD v2: 10-69955547-C-CT
• gnomAD v3: 10-68195790-C-CT
• gnomAD v4: 10-68195790-C-CT
• COSMIC: COSN23300599
• MyVariant Identifiers: chr10:g.69955547_69955548insT (hg19) ; chr10:g.68195790_68195791insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195799dup , CM000672.2:g.68195799dup	GRCh38
NC_000010.10:g.69955556dup , CM000672.1:g.69955556dup	GRCh37
NC_000010.9:g.69625562dup	NCBI36
NG_032118.1:g.94683dup , LRG_410:g.94683dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+267dup	ENSP00000346369.2:n.2333+267dup
ENST00000540630.6:c.3212+267dup	ENSP00000441668.3:n.3212+267dup
ENST00000613327.5:c.3158+267dup	ENSP00000480757.2:n.3158+267dup
ENST00000688812.1:c.*421+267dup	ENSP00000510658.1:n.*421+267dup
ENST00000690544.1:c.*2429+267dup	ENSP00000508989.1:n.*2429+267dup
ENST00000358913.10:c.3158+267dup MANE Select	ENSP00000351790.5:n.3158+267dup
ENST00000354393.6:c.2333+267dup	ENSP00000346369.2:n.2333+267dup
ENST00000358913.9:c.3158+267dup	ENSP00000351790.5:n.3158+267dup
ENST00000540630.5:c.3158+267dup	ENSP00000441668.2:n.3158+267dup
ENST00000613327.4:c.2276+267dup	ENSP00000480757.1:n.2276+267dup
NM_001256267.1:c.3158+267dup	NP_001243196.1:n.3158+267dup
NM_001256268.1:c.2276+267dup	NP_001243197.1:n.2276+267dup
NM_032578.3:c.3158+267dup , LRG_410t1:c.3158+267dup	NP_115967.2:n.3158+267dup
NR_045662.3:n.2585+267dup
NR_045663.3:n.3287+267dup
XM_006718043.2:c.3212+267dup	XP_006718106.1:n.3212+267dup
XM_011540292.1:c.3188+267dup	XP_011538594.1:n.3188+267dup
XM_017016833.1:c.3236+267dup	XP_016872322.1:n.3236+267dup
XM_017016834.2:c.3158+267dup	XP_016872323.1:n.3158+267dup
XM_024448236.1:c.2036+267dup	XP_024304004.1:n.2036+267dup
NR_045662.4:n.2695+267dup
NR_045663.4:n.3232+267dup
NM_001256267.2:c.3158+267dup	NP_001243196.1:n.3158+267dup
NM_001256268.2:c.2276+267dup	NP_001243197.1:n.2276+267dup
NM_032578.4:c.3158+267dup MANE Select	NP_115967.2:n.3158+267dup