Canonical Allele Identifier: CA376858877

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959131G>T (hg19) ; chr10:g.68199374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199374G>T , CM000672.2:g.68199374G>T	GRCh38
NC_000010.10:g.69959131G>T , CM000672.1:g.69959131G>T	GRCh37
NC_000010.9:g.69629137G>T	NCBI36
NG_032118.1:g.98258G>T , LRG_410:g.98258G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2467G>T	ENSP00000346369.2:p.Gly823Cys
ENST00000540630.6:c.3346G>T	ENSP00000441668.3:p.Gly1116Cys
ENST00000613327.5:c.3292G>T	ENSP00000480757.2:p.Gly1098Cys
ENST00000688812.1:c.*555G>T	ENSP00000510658.1:n.*555G>T
ENST00000690544.1:c.*2563G>T	ENSP00000508989.1:n.*2563G>T
ENST00000358913.10:c.3292G>T MANE Select	ENSP00000351790.5:p.Gly1098Cys
ENST00000354393.6:c.2467G>T	ENSP00000346369.2:p.Gly823Cys
ENST00000358913.9:c.3292G>T	ENSP00000351790.5:p.Gly1098Cys
ENST00000540630.5:c.3292G>T	ENSP00000441668.2:p.Gly1098Cys
ENST00000613327.4:c.2410G>T	ENSP00000480757.1:p.Gly804Cys
NM_001256267.1:c.3292G>T	NP_001243196.1:p.Gly1098Cys
NM_001256268.1:c.2410G>T	NP_001243197.1:p.Gly804Cys
NM_032578.3:c.3292G>T , LRG_410t1:c.3292G>T	NP_115967.2:p.Gly1098Cys
NR_045662.3:n.2719G>T
NR_045663.3:n.3421G>T
XM_006718043.2:c.3346G>T	XP_006718106.1:p.Gly1116Cys
XM_011540292.1:c.3322G>T	XP_011538594.1:p.Gly1108Cys
XR_946029.1:n.1804-99C>A
XM_017016833.1:c.3370G>T	XP_016872322.1:p.Gly1124Cys
XM_017016834.2:c.3292G>T	XP_016872323.1:p.Gly1098Cys
XM_024448236.1:c.2170G>T	XP_024304004.1:p.Gly724Cys
NR_045662.4:n.2829G>T
NR_045663.4:n.3366G>T
NM_001256267.2:c.3292G>T	NP_001243196.1:p.Gly1098Cys
NM_001256268.2:c.2410G>T	NP_001243197.1:p.Gly804Cys
NM_032578.4:c.3292G>T MANE Select	NP_115967.2:p.Gly1098Cys