Canonical Allele Identifier: CA376859258

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959246T>C (hg19) ; chr10:g.68199489T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199489T>C , CM000672.2:g.68199489T>C	GRCh38
NC_000010.10:g.69959246T>C , CM000672.1:g.69959246T>C	GRCh37
NC_000010.9:g.69629252T>C	NCBI36
NG_032118.1:g.98373T>C , LRG_410:g.98373T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2582T>C	ENSP00000346369.2:p.Leu861Pro
ENST00000540630.6:c.3461T>C	ENSP00000441668.3:p.Leu1154Pro
ENST00000613327.5:c.3407T>C	ENSP00000480757.2:p.Leu1136Pro
ENST00000688812.1:c.*670T>C	ENSP00000510658.1:n.*670T>C
ENST00000690544.1:c.*2678T>C	ENSP00000508989.1:n.*2678T>C
ENST00000358913.10:c.3407T>C MANE Select	ENSP00000351790.5:p.Leu1136Pro
ENST00000354393.6:c.2582T>C	ENSP00000346369.2:p.Leu861Pro
ENST00000358913.9:c.3407T>C	ENSP00000351790.5:p.Leu1136Pro
ENST00000540630.5:c.3407T>C	ENSP00000441668.2:p.Leu1136Pro
ENST00000613327.4:c.2525T>C	ENSP00000480757.1:p.Leu842Pro
NM_001256267.1:c.3407T>C	NP_001243196.1:p.Leu1136Pro
NM_001256268.1:c.2525T>C	NP_001243197.1:p.Leu842Pro
NM_032578.3:c.3407T>C , LRG_410t1:c.3407T>C	NP_115967.2:p.Leu1136Pro
NR_045662.3:n.2834T>C
NR_045663.3:n.3536T>C
XM_006718043.2:c.3461T>C	XP_006718106.1:p.Leu1154Pro
XM_011540292.1:c.3437T>C	XP_011538594.1:p.Leu1146Pro
XR_946029.1:n.1804-214A>G
XM_017016833.1:c.3485T>C	XP_016872322.1:p.Leu1162Pro
XM_017016834.2:c.3407T>C	XP_016872323.1:p.Leu1136Pro
XM_024448236.1:c.2285T>C	XP_024304004.1:p.Leu762Pro
NR_045662.4:n.2944T>C
NR_045663.4:n.3481T>C
NM_001256267.2:c.3407T>C	NP_001243196.1:p.Leu1136Pro
NM_001256268.2:c.2525T>C	NP_001243197.1:p.Leu842Pro
NM_032578.4:c.3407T>C MANE Select	NP_115967.2:p.Leu1136Pro