Canonical Allele Identifier: CA376858944

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959150T>C (hg19) ; chr10:g.68199393T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199393T>C , CM000672.2:g.68199393T>C	GRCh38
NC_000010.10:g.69959150T>C , CM000672.1:g.69959150T>C	GRCh37
NC_000010.9:g.69629156T>C	NCBI36
NG_032118.1:g.98277T>C , LRG_410:g.98277T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2486T>C	ENSP00000346369.2:p.Leu829Pro
ENST00000540630.6:c.3365T>C	ENSP00000441668.3:p.Leu1122Pro
ENST00000613327.5:c.3311T>C	ENSP00000480757.2:p.Leu1104Pro
ENST00000688812.1:c.*574T>C	ENSP00000510658.1:n.*574T>C
ENST00000690544.1:c.*2582T>C	ENSP00000508989.1:n.*2582T>C
ENST00000358913.10:c.3311T>C MANE Select	ENSP00000351790.5:p.Leu1104Pro
ENST00000354393.6:c.2486T>C	ENSP00000346369.2:p.Leu829Pro
ENST00000358913.9:c.3311T>C	ENSP00000351790.5:p.Leu1104Pro
ENST00000540630.5:c.3311T>C	ENSP00000441668.2:p.Leu1104Pro
ENST00000613327.4:c.2429T>C	ENSP00000480757.1:p.Leu810Pro
NM_001256267.1:c.3311T>C	NP_001243196.1:p.Leu1104Pro
NM_001256268.1:c.2429T>C	NP_001243197.1:p.Leu810Pro
NM_032578.3:c.3311T>C , LRG_410t1:c.3311T>C	NP_115967.2:p.Leu1104Pro
NR_045662.3:n.2738T>C
NR_045663.3:n.3440T>C
XM_006718043.2:c.3365T>C	XP_006718106.1:p.Leu1122Pro
XM_011540292.1:c.3341T>C	XP_011538594.1:p.Leu1114Pro
XR_946029.1:n.1804-118A>G
XM_017016833.1:c.3389T>C	XP_016872322.1:p.Leu1130Pro
XM_017016834.2:c.3311T>C	XP_016872323.1:p.Leu1104Pro
XM_024448236.1:c.2189T>C	XP_024304004.1:p.Leu730Pro
NR_045662.4:n.2848T>C
NR_045663.4:n.3385T>C
NM_001256267.2:c.3311T>C	NP_001243196.1:p.Leu1104Pro
NM_001256268.2:c.2429T>C	NP_001243197.1:p.Leu810Pro
NM_032578.4:c.3311T>C MANE Select	NP_115967.2:p.Leu1104Pro