Canonical Allele Identifier: CA376857536

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955254T>G (hg19) ; chr10:g.68195497T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195497T>G , CM000672.2:g.68195497T>G	GRCh38
NC_000010.10:g.69955254T>G , CM000672.1:g.69955254T>G	GRCh37
NC_000010.9:g.69625260T>G	NCBI36
NG_032118.1:g.94381T>G , LRG_410:g.94381T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2298T>G	ENSP00000346369.2:p.Ile766Met
ENST00000540630.6:c.3177T>G	ENSP00000441668.3:p.Ile1059Met
ENST00000613327.5:c.3123T>G	ENSP00000480757.2:p.Ile1041Met
ENST00000688812.1:c.*386T>G	ENSP00000510658.1:n.*386T>G
ENST00000690544.1:c.*2394T>G	ENSP00000508989.1:n.*2394T>G
ENST00000358913.10:c.3123T>G MANE Select	ENSP00000351790.5:p.Ile1041Met
ENST00000354393.6:c.2298T>G	ENSP00000346369.2:p.Ile766Met
ENST00000358913.9:c.3123T>G	ENSP00000351790.5:p.Ile1041Met
ENST00000540630.5:c.3123T>G	ENSP00000441668.2:p.Ile1041Met
ENST00000613327.4:c.2241T>G	ENSP00000480757.1:p.Ile747Met
NM_001256267.1:c.3123T>G	NP_001243196.1:p.Ile1041Met
NM_001256268.1:c.2241T>G	NP_001243197.1:p.Ile747Met
NM_032578.3:c.3123T>G , LRG_410t1:c.3123T>G	NP_115967.2:p.Ile1041Met
NR_045662.3:n.2550T>G
NR_045663.3:n.3252T>G
XM_006718043.2:c.3177T>G	XP_006718106.1:p.Ile1059Met
XM_011540292.1:c.3153T>G	XP_011538594.1:p.Ile1051Met
XM_017016833.1:c.3201T>G	XP_016872322.1:p.Ile1067Met
XM_017016834.2:c.3123T>G	XP_016872323.1:p.Ile1041Met
XM_024448236.1:c.2001T>G	XP_024304004.1:p.Ile667Met
NR_045662.4:n.2660T>G
NR_045663.4:n.3197T>G
NM_001256267.2:c.3123T>G	NP_001243196.1:p.Ile1041Met
NM_001256268.2:c.2241T>G	NP_001243197.1:p.Ile747Met
NM_032578.4:c.3123T>G MANE Select	NP_115967.2:p.Ile1041Met