Canonical Allele Identifier: CA469812131

Gene: MYPN

Linked Data

• dbSNP Id: rs1222910157
• MyVariant Identifiers: chr10:g.69955218C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195461C>T , CM000672.2:g.68195461C>T	GRCh38
NC_000010.10:g.69955218C>T , CM000672.1:g.69955218C>T	GRCh37
NC_000010.9:g.69625224C>T	NCBI36
NG_032118.1:g.94345C>T , LRG_410:g.94345C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354393.7:c.2262C>T	ENSP00000346369.2:p.Ser754=
ENST00000540630.6:c.3141C>T	ENSP00000441668.3:p.Ser1047=
ENST00000613327.5:c.3087C>T	ENSP00000480757.2:p.Ser1029=
ENST00000688812.1:c.*350C>T	ENSP00000510658.1:n.*350C>T
ENST00000690544.1:c.*2358C>T	ENSP00000508989.1:n.*2358C>T
ENST00000358913.10:c.3087C>T MANE Select	ENSP00000351790.5:p.Ser1029=
ENST00000354393.6:c.2262C>T	ENSP00000346369.2:p.Ser754=
ENST00000358913.9:c.3087C>T	ENSP00000351790.5:p.Ser1029=
ENST00000540630.5:c.3087C>T	ENSP00000441668.2:p.Ser1029=
ENST00000613327.4:c.2205C>T	ENSP00000480757.1:p.Ser735=
NM_001256267.1:c.3087C>T	NP_001243196.1:p.Ser1029=
NM_001256268.1:c.2205C>T	NP_001243197.1:p.Ser735=
NM_032578.3:c.3087C>T , LRG_410t1:c.3087C>T	NP_115967.2:p.Ser1029=
NR_045662.3:n.2514C>T
NR_045663.3:n.3216C>T
XM_006718043.2:c.3141C>T	XP_006718106.1:p.Ser1047=
XM_011540292.1:c.3117C>T	XP_011538594.1:p.Ser1039=
XM_017016833.1:c.3165C>T	XP_016872322.1:p.Ser1055=
XM_017016834.2:c.3087C>T	XP_016872323.1:p.Ser1029=
XM_024448236.1:c.1965C>T	XP_024304004.1:p.Ser655=
NR_045662.4:n.2624C>T
NR_045663.4:n.3161C>T
NM_001256267.2:c.3087C>T	NP_001243196.1:p.Ser1029=
NM_001256268.2:c.2205C>T	NP_001243197.1:p.Ser735=
NM_032578.4:c.3087C>T MANE Select	NP_115967.2:p.Ser1029=