Canonical Allele Identifier: CA376857562

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955258A>T (hg19) ; chr10:g.68195501A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195501A>T , CM000672.2:g.68195501A>T	GRCh38
NC_000010.10:g.69955258A>T , CM000672.1:g.69955258A>T	GRCh37
NC_000010.9:g.69625264A>T	NCBI36
NG_032118.1:g.94385A>T , LRG_410:g.94385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2302A>T	ENSP00000346369.2:p.Ser768Cys
ENST00000540630.6:c.3181A>T	ENSP00000441668.3:p.Ser1061Cys
ENST00000613327.5:c.3127A>T	ENSP00000480757.2:p.Ser1043Cys
ENST00000688812.1:c.*390A>T	ENSP00000510658.1:n.*390A>T
ENST00000690544.1:c.*2398A>T	ENSP00000508989.1:n.*2398A>T
ENST00000358913.10:c.3127A>T MANE Select	ENSP00000351790.5:p.Ser1043Cys
ENST00000354393.6:c.2302A>T	ENSP00000346369.2:p.Ser768Cys
ENST00000358913.9:c.3127A>T	ENSP00000351790.5:p.Ser1043Cys
ENST00000540630.5:c.3127A>T	ENSP00000441668.2:p.Ser1043Cys
ENST00000613327.4:c.2245A>T	ENSP00000480757.1:p.Ser749Cys
NM_001256267.1:c.3127A>T	NP_001243196.1:p.Ser1043Cys
NM_001256268.1:c.2245A>T	NP_001243197.1:p.Ser749Cys
NM_032578.3:c.3127A>T , LRG_410t1:c.3127A>T	NP_115967.2:p.Ser1043Cys
NR_045662.3:n.2554A>T
NR_045663.3:n.3256A>T
XM_006718043.2:c.3181A>T	XP_006718106.1:p.Ser1061Cys
XM_011540292.1:c.3157A>T	XP_011538594.1:p.Ser1053Cys
XM_017016833.1:c.3205A>T	XP_016872322.1:p.Ser1069Cys
XM_017016834.2:c.3127A>T	XP_016872323.1:p.Ser1043Cys
XM_024448236.1:c.2005A>T	XP_024304004.1:p.Ser669Cys
NR_045662.4:n.2664A>T
NR_045663.4:n.3201A>T
NM_001256267.2:c.3127A>T	NP_001243196.1:p.Ser1043Cys
NM_001256268.2:c.2245A>T	NP_001243197.1:p.Ser749Cys
NM_032578.4:c.3127A>T MANE Select	NP_115967.2:p.Ser1043Cys