Canonical Allele Identifier: CA2609373535

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199297-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199300del , CM000672.2:g.68199300del	GRCh38
NC_000010.10:g.69959057del , CM000672.1:g.69959057del	GRCh37
NC_000010.9:g.69629063del	NCBI36
NG_032118.1:g.98184del , LRG_410:g.98184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2461-68del	ENSP00000346369.2:n.2461-68del
ENST00000540630.6:c.3340-68del	ENSP00000441668.3:n.3340-68del
ENST00000613327.5:c.3286-68del	ENSP00000480757.2:n.3286-68del
ENST00000688812.1:c.*549-68del	ENSP00000510658.1:n.*549-68del
ENST00000690544.1:c.*2557-68del	ENSP00000508989.1:n.*2557-68del
ENST00000358913.10:c.3286-68del MANE Select	ENSP00000351790.5:n.3286-68del
ENST00000354393.6:c.2461-68del	ENSP00000346369.2:n.2461-68del
ENST00000358913.9:c.3286-68del	ENSP00000351790.5:n.3286-68del
ENST00000540630.5:c.3286-68del	ENSP00000441668.2:n.3286-68del
ENST00000613327.4:c.2404-68del	ENSP00000480757.1:n.2404-68del
NM_001256267.1:c.3286-68del	NP_001243196.1:n.3286-68del
NM_001256268.1:c.2404-68del	NP_001243197.1:n.2404-68del
NM_032578.3:c.3286-68del , LRG_410t1:c.3286-68del	NP_115967.2:n.3286-68del
NR_045662.3:n.2713-68del
NR_045663.3:n.3415-68del
XM_006718043.2:c.3340-68del	XP_006718106.1:n.3340-68del
XM_011540292.1:c.3316-68del	XP_011538594.1:n.3316-68del
XR_946029.1:n.1804-23del
XM_017016833.1:c.3364-68del	XP_016872322.1:n.3364-68del
XM_017016834.2:c.3286-68del	XP_016872323.1:n.3286-68del
XM_024448236.1:c.2164-68del	XP_024304004.1:n.2164-68del
NR_045662.4:n.2823-68del
NR_045663.4:n.3360-68del
NM_001256267.2:c.3286-68del	NP_001243196.1:n.3286-68del
NM_001256268.2:c.2404-68del	NP_001243197.1:n.2404-68del
NM_032578.4:c.3286-68del MANE Select	NP_115967.2:n.3286-68del