Canonical Allele Identifier: CA667798749

Gene: MYPN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197270del , CM000672.2:g.68197270del	GRCh38
NC_000010.10:g.69957027del , CM000672.1:g.69957027del	GRCh37
NC_000010.9:g.69627033del	NCBI36
NG_032118.1:g.96154del , LRG_410:g.96154del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2334-82del	ENSP00000346369.2:n.2334-82del
ENST00000540630.6:c.3213-82del	ENSP00000441668.3:n.3213-82del
ENST00000613327.5:c.3159-82del	ENSP00000480757.2:n.3159-82del
ENST00000688812.1:c.*422-82del	ENSP00000510658.1:n.*422-82del
ENST00000690544.1:c.*2430-82del	ENSP00000508989.1:n.*2430-82del
ENST00000358913.10:c.3159-82del MANE Select	ENSP00000351790.5:n.3159-82del
ENST00000354393.6:c.2334-82del	ENSP00000346369.2:n.2334-82del
ENST00000358913.9:c.3159-82del	ENSP00000351790.5:n.3159-82del
ENST00000540630.5:c.3159-82del	ENSP00000441668.2:n.3159-82del
ENST00000613327.4:c.2277-82del	ENSP00000480757.1:n.2277-82del
NM_001256267.1:c.3159-82del	NP_001243196.1:n.3159-82del
NM_001256268.1:c.2277-82del	NP_001243197.1:n.2277-82del
NM_032578.3:c.3159-82del , LRG_410t1:c.3159-82del	NP_115967.2:n.3159-82del
NR_045662.3:n.2586-82del
NR_045663.3:n.3288-82del
XM_006718043.2:c.3213-82del	XP_006718106.1:n.3213-82del
XM_011540292.1:c.3189-82del	XP_011538594.1:n.3189-82del
XM_017016833.1:c.3237-82del	XP_016872322.1:n.3237-82del
XM_017016834.2:c.3159-82del	XP_016872323.1:n.3159-82del
XM_024448236.1:c.2037-82del	XP_024304004.1:n.2037-82del
NR_045662.4:n.2696-82del
NR_045663.4:n.3233-82del
NM_001256267.2:c.3159-82del	NP_001243196.1:n.3159-82del
NM_001256268.2:c.2277-82del	NP_001243197.1:n.2277-82del
NM_032578.4:c.3159-82del MANE Select	NP_115967.2:n.3159-82del