Canonical Allele Identifier: CA1917225541

Gene: MYPN

Linked Data

• dbSNP Id: rs1190113003
• gnomAD v4: 10-68195397-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195403dup , CM000672.2:g.68195403dup	GRCh38
NC_000010.10:g.69955160dup , CM000672.1:g.69955160dup	GRCh37
NC_000010.9:g.69625166dup	NCBI36
NG_032118.1:g.94287dup , LRG_410:g.94287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2251-47dup	ENSP00000346369.2:n.2251-47dup
ENST00000540630.6:c.3130-47dup	ENSP00000441668.3:n.3130-47dup
ENST00000613327.5:c.3076-47dup	ENSP00000480757.2:n.3076-47dup
ENST00000688812.1:c.*339-47dup	ENSP00000510658.1:n.*339-47dup
ENST00000690544.1:c.*2347-47dup	ENSP00000508989.1:n.*2347-47dup
ENST00000358913.10:c.3076-47dup MANE Select	ENSP00000351790.5:n.3076-47dup
ENST00000354393.6:c.2251-47dup	ENSP00000346369.2:n.2251-47dup
ENST00000358913.9:c.3076-47dup	ENSP00000351790.5:n.3076-47dup
ENST00000540630.5:c.3076-47dup	ENSP00000441668.2:n.3076-47dup
ENST00000613327.4:c.2194-47dup	ENSP00000480757.1:n.2194-47dup
NM_001256267.1:c.3076-47dup	NP_001243196.1:n.3076-47dup
NM_001256268.1:c.2194-47dup	NP_001243197.1:n.2194-47dup
NM_032578.3:c.3076-47dup , LRG_410t1:c.3076-47dup	NP_115967.2:n.3076-47dup
NR_045662.3:n.2503-47dup
NR_045663.3:n.3205-47dup
XM_006718043.2:c.3130-47dup	XP_006718106.1:n.3130-47dup
XM_011540292.1:c.3106-47dup	XP_011538594.1:n.3106-47dup
XM_017016833.1:c.3154-47dup	XP_016872322.1:n.3154-47dup
XM_017016834.2:c.3076-47dup	XP_016872323.1:n.3076-47dup
XM_024448236.1:c.1954-47dup	XP_024304004.1:n.1954-47dup
NR_045662.4:n.2613-47dup
NR_045663.4:n.3150-47dup
NM_001256267.2:c.3076-47dup	NP_001243196.1:n.3076-47dup
NM_001256268.2:c.2194-47dup	NP_001243197.1:n.2194-47dup
NM_032578.4:c.3076-47dup MANE Select	NP_115967.2:n.3076-47dup