Canonical Allele Identifier: CA2609373133

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195550-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195554_68195555del , CM000672.2:g.68195554_68195555del	GRCh38
NC_000010.10:g.69955311_69955312del , CM000672.1:g.69955311_69955312del	GRCh37
NC_000010.9:g.69625317_69625318del	NCBI36
NG_032118.1:g.94438_94439del , LRG_410:g.94438_94439del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+22_2333+23del	ENSP00000346369.2:n.2333+22_2333+23del
ENST00000540630.6:c.3212+22_3212+23del	ENSP00000441668.3:n.3212+22_3212+23del
ENST00000613327.5:c.3158+22_3158+23del	ENSP00000480757.2:n.3158+22_3158+23del
ENST00000688812.1:c.*421+22_*421+23del	ENSP00000510658.1:n.*421+22_*421+23del
ENST00000690544.1:c.*2429+22_*2429+23del	ENSP00000508989.1:n.*2429+22_*2429+23del
ENST00000358913.10:c.3158+22_3158+23del MANE Select	ENSP00000351790.5:n.3158+22_3158+23del
ENST00000354393.6:c.2333+22_2333+23del	ENSP00000346369.2:n.2333+22_2333+23del
ENST00000358913.9:c.3158+22_3158+23del	ENSP00000351790.5:n.3158+22_3158+23del
ENST00000540630.5:c.3158+22_3158+23del	ENSP00000441668.2:n.3158+22_3158+23del
ENST00000613327.4:c.2276+22_2276+23del	ENSP00000480757.1:n.2276+22_2276+23del
NM_001256267.1:c.3158+22_3158+23del	NP_001243196.1:n.3158+22_3158+23del
NM_001256268.1:c.2276+22_2276+23del	NP_001243197.1:n.2276+22_2276+23del
NM_032578.3:c.3158+22_3158+23del , LRG_410t1:c.3158+22_3158+23del	NP_115967.2:n.3158+22_3158+23del
NR_045662.3:n.2585+22_2585+23del
NR_045663.3:n.3287+22_3287+23del
XM_006718043.2:c.3212+22_3212+23del	XP_006718106.1:n.3212+22_3212+23del
XM_011540292.1:c.3188+22_3188+23del	XP_011538594.1:n.3188+22_3188+23del
XM_017016833.1:c.3236+22_3236+23del	XP_016872322.1:n.3236+22_3236+23del
XM_017016834.2:c.3158+22_3158+23del	XP_016872323.1:n.3158+22_3158+23del
XM_024448236.1:c.2036+22_2036+23del	XP_024304004.1:n.2036+22_2036+23del
NR_045662.4:n.2695+22_2695+23del
NR_045663.4:n.3232+22_3232+23del
NM_001256267.2:c.3158+22_3158+23del	NP_001243196.1:n.3158+22_3158+23del
NM_001256268.2:c.2276+22_2276+23del	NP_001243197.1:n.2276+22_2276+23del
NM_032578.4:c.3158+22_3158+23del MANE Select	NP_115967.2:n.3158+22_3158+23del