Canonical Allele Identifier: CA376857314

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955219T>G (hg19) ; chr10:g.68195462T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195462T>G , CM000672.2:g.68195462T>G	GRCh38
NC_000010.10:g.69955219T>G , CM000672.1:g.69955219T>G	GRCh37
NC_000010.9:g.69625225T>G	NCBI36
NG_032118.1:g.94346T>G , LRG_410:g.94346T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2263T>G	ENSP00000346369.2:p.Cys755Gly
ENST00000540630.6:c.3142T>G	ENSP00000441668.3:p.Cys1048Gly
ENST00000613327.5:c.3088T>G	ENSP00000480757.2:p.Cys1030Gly
ENST00000688812.1:c.*351T>G	ENSP00000510658.1:n.*351T>G
ENST00000690544.1:c.*2359T>G	ENSP00000508989.1:n.*2359T>G
ENST00000358913.10:c.3088T>G MANE Select	ENSP00000351790.5:p.Cys1030Gly
ENST00000354393.6:c.2263T>G	ENSP00000346369.2:p.Cys755Gly
ENST00000358913.9:c.3088T>G	ENSP00000351790.5:p.Cys1030Gly
ENST00000540630.5:c.3088T>G	ENSP00000441668.2:p.Cys1030Gly
ENST00000613327.4:c.2206T>G	ENSP00000480757.1:p.Cys736Gly
NM_001256267.1:c.3088T>G	NP_001243196.1:p.Cys1030Gly
NM_001256268.1:c.2206T>G	NP_001243197.1:p.Cys736Gly
NM_032578.3:c.3088T>G , LRG_410t1:c.3088T>G	NP_115967.2:p.Cys1030Gly
NR_045662.3:n.2515T>G
NR_045663.3:n.3217T>G
XM_006718043.2:c.3142T>G	XP_006718106.1:p.Cys1048Gly
XM_011540292.1:c.3118T>G	XP_011538594.1:p.Cys1040Gly
XM_017016833.1:c.3166T>G	XP_016872322.1:p.Cys1056Gly
XM_017016834.2:c.3088T>G	XP_016872323.1:p.Cys1030Gly
XM_024448236.1:c.1966T>G	XP_024304004.1:p.Cys656Gly
NR_045662.4:n.2625T>G
NR_045663.4:n.3162T>G
NM_001256267.2:c.3088T>G	NP_001243196.1:p.Cys1030Gly
NM_001256268.2:c.2206T>G	NP_001243197.1:p.Cys736Gly
NM_032578.4:c.3088T>G MANE Select	NP_115967.2:p.Cys1030Gly