Canonical Allele Identifier: CA1917225519

Gene: MYPN

Linked Data

• dbSNP Id: rs2043586529

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195347_68195351del , CM000672.2:g.68195347_68195351del	GRCh38
NC_000010.10:g.69955104_69955108del , CM000672.1:g.69955104_69955108del	GRCh37
NC_000010.9:g.69625110_69625114del	NCBI36
NG_032118.1:g.94231_94235del , LRG_410:g.94231_94235del

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2251-103_2251-99del	ENSP00000346369.2:n.2251-103_2251-99del
ENST00000540630.6:c.3130-103_3130-99del	ENSP00000441668.3:n.3130-103_3130-99del
ENST00000613327.5:c.3076-103_3076-99del	ENSP00000480757.2:n.3076-103_3076-99del
ENST00000688812.1:c.*339-103_*339-99del	ENSP00000510658.1:n.*339-103_*339-99del
ENST00000690544.1:c.*2347-103_*2347-99del	ENSP00000508989.1:n.*2347-103_*2347-99del...
ENST00000358913.10:c.3076-103_3076-99del MANE Select	ENSP00000351790.5:n.3076-103_3076-99del
ENST00000354393.6:c.2251-103_2251-99del	ENSP00000346369.2:n.2251-103_2251-99del
ENST00000358913.9:c.3076-103_3076-99del	ENSP00000351790.5:n.3076-103_3076-99del
ENST00000540630.5:c.3076-103_3076-99del	ENSP00000441668.2:n.3076-103_3076-99del
ENST00000613327.4:c.2194-103_2194-99del	ENSP00000480757.1:n.2194-103_2194-99del
NM_001256267.1:c.3076-103_3076-99del	NP_001243196.1:n.3076-103_3076-99del
NM_001256268.1:c.2194-103_2194-99del	NP_001243197.1:n.2194-103_2194-99del
NM_032578.3:c.3076-103_3076-99del , LRG_410t1:c.3076-103_3076-99del	NP_115967.2:n.3076-103_3076-99del
NR_045662.3:n.2503-103_2503-99del
NR_045663.3:n.3205-103_3205-99del
XM_006718043.2:c.3130-103_3130-99del	XP_006718106.1:n.3130-103_3130-99del
XM_011540292.1:c.3106-103_3106-99del	XP_011538594.1:n.3106-103_3106-99del
XM_017016833.1:c.3154-103_3154-99del	XP_016872322.1:n.3154-103_3154-99del
XM_017016834.2:c.3076-103_3076-99del	XP_016872323.1:n.3076-103_3076-99del
XM_024448236.1:c.1954-103_1954-99del	XP_024304004.1:n.1954-103_1954-99del
NR_045662.4:n.2613-103_2613-99del
NR_045663.4:n.3150-103_3150-99del
NM_001256267.2:c.3076-103_3076-99del	NP_001243196.1:n.3076-103_3076-99del
NM_001256268.2:c.2194-103_2194-99del	NP_001243197.1:n.2194-103_2194-99del
NM_032578.4:c.3076-103_3076-99del MANE Select	NP_115967.2:n.3076-103_3076-99del