Canonical Allele Identifier: CA469812137

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955224T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195467T>G , CM000672.2:g.68195467T>G	GRCh38
NC_000010.10:g.69955224T>G , CM000672.1:g.69955224T>G	GRCh37
NC_000010.9:g.69625230T>G	NCBI36
NG_032118.1:g.94351T>G , LRG_410:g.94351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2268T>G	ENSP00000346369.2:p.Ser756=
ENST00000540630.6:c.3147T>G	ENSP00000441668.3:p.Ser1049=
ENST00000613327.5:c.3093T>G	ENSP00000480757.2:p.Ser1031=
ENST00000688812.1:c.*356T>G	ENSP00000510658.1:n.*356T>G
ENST00000690544.1:c.*2364T>G	ENSP00000508989.1:n.*2364T>G
ENST00000358913.10:c.3093T>G MANE Select	ENSP00000351790.5:p.Ser1031=
ENST00000354393.6:c.2268T>G	ENSP00000346369.2:p.Ser756=
ENST00000358913.9:c.3093T>G	ENSP00000351790.5:p.Ser1031=
ENST00000540630.5:c.3093T>G	ENSP00000441668.2:p.Ser1031=
ENST00000613327.4:c.2211T>G	ENSP00000480757.1:p.Ser737=
NM_001256267.1:c.3093T>G	NP_001243196.1:p.Ser1031=
NM_001256268.1:c.2211T>G	NP_001243197.1:p.Ser737=
NM_032578.3:c.3093T>G , LRG_410t1:c.3093T>G	NP_115967.2:p.Ser1031=
NR_045662.3:n.2520T>G
NR_045663.3:n.3222T>G
XM_006718043.2:c.3147T>G	XP_006718106.1:p.Ser1049=
XM_011540292.1:c.3123T>G	XP_011538594.1:p.Ser1041=
XM_017016833.1:c.3171T>G	XP_016872322.1:p.Ser1057=
XM_017016834.2:c.3093T>G	XP_016872323.1:p.Ser1031=
XM_024448236.1:c.1971T>G	XP_024304004.1:p.Ser657=
NR_045662.4:n.2630T>G
NR_045663.4:n.3167T>G
NM_001256267.2:c.3093T>G	NP_001243196.1:p.Ser1031=
NM_001256268.2:c.2211T>G	NP_001243197.1:p.Ser737=
NM_032578.4:c.3093T>G MANE Select	NP_115967.2:p.Ser1031=