Canonical Allele Identifier: CA376859243

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959239G>T (hg19) ; chr10:g.68199482G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199482G>T , CM000672.2:g.68199482G>T	GRCh38
NC_000010.10:g.69959239G>T , CM000672.1:g.69959239G>T	GRCh37
NC_000010.9:g.69629245G>T	NCBI36
NG_032118.1:g.98366G>T , LRG_410:g.98366G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2575G>T	ENSP00000346369.2:p.Asp859Tyr
ENST00000540630.6:c.3454G>T	ENSP00000441668.3:p.Asp1152Tyr
ENST00000613327.5:c.3400G>T	ENSP00000480757.2:p.Asp1134Tyr
ENST00000688812.1:c.*663G>T	ENSP00000510658.1:n.*663G>T
ENST00000690544.1:c.*2671G>T	ENSP00000508989.1:n.*2671G>T
ENST00000358913.10:c.3400G>T MANE Select	ENSP00000351790.5:p.Asp1134Tyr
ENST00000354393.6:c.2575G>T	ENSP00000346369.2:p.Asp859Tyr
ENST00000358913.9:c.3400G>T	ENSP00000351790.5:p.Asp1134Tyr
ENST00000540630.5:c.3400G>T	ENSP00000441668.2:p.Asp1134Tyr
ENST00000613327.4:c.2518G>T	ENSP00000480757.1:p.Asp840Tyr
NM_001256267.1:c.3400G>T	NP_001243196.1:p.Asp1134Tyr
NM_001256268.1:c.2518G>T	NP_001243197.1:p.Asp840Tyr
NM_032578.3:c.3400G>T , LRG_410t1:c.3400G>T	NP_115967.2:p.Asp1134Tyr
NR_045662.3:n.2827G>T
NR_045663.3:n.3529G>T
XM_006718043.2:c.3454G>T	XP_006718106.1:p.Asp1152Tyr
XM_011540292.1:c.3430G>T	XP_011538594.1:p.Asp1144Tyr
XR_946029.1:n.1804-207C>A
XM_017016833.1:c.3478G>T	XP_016872322.1:p.Asp1160Tyr
XM_017016834.2:c.3400G>T	XP_016872323.1:p.Asp1134Tyr
XM_024448236.1:c.2278G>T	XP_024304004.1:p.Asp760Tyr
NR_045662.4:n.2937G>T
NR_045663.4:n.3474G>T
NM_001256267.2:c.3400G>T	NP_001243196.1:p.Asp1134Tyr
NM_001256268.2:c.2518G>T	NP_001243197.1:p.Asp840Tyr
NM_032578.4:c.3400G>T MANE Select	NP_115967.2:p.Asp1134Tyr