Canonical Allele Identifier: CA376860055

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69961654C>T (hg19) ; chr10:g.68201897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68201897C>T , CM000672.2:g.68201897C>T	GRCh38
NC_000010.10:g.69961654C>T , CM000672.1:g.69961654C>T	GRCh37
NC_000010.9:g.69631660C>T	NCBI36
NG_032118.1:g.100781C>T , LRG_410:g.100781C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2737C>T	ENSP00000346369.2:p.Pro913Ser
ENST00000540630.6:c.3616C>T	ENSP00000441668.3:p.Pro1206Ser
ENST00000613327.5:c.3562C>T	ENSP00000480757.2:p.Pro1188Ser
ENST00000688812.1:c.*825C>T	ENSP00000510658.1:n.*825C>T
ENST00000690544.1:c.*2833C>T	ENSP00000508989.1:n.*2833C>T
ENST00000358913.10:c.3562C>T MANE Select	ENSP00000351790.5:p.Pro1188Ser
ENST00000354393.6:c.2737C>T	ENSP00000346369.2:p.Pro913Ser
ENST00000358913.9:c.3562C>T	ENSP00000351790.5:p.Pro1188Ser
ENST00000540630.5:c.3562C>T	ENSP00000441668.2:p.Pro1188Ser
ENST00000613327.4:c.2680C>T	ENSP00000480757.1:p.Pro894Ser
NM_001256267.1:c.3562C>T	NP_001243196.1:p.Pro1188Ser
NM_001256268.1:c.2680C>T	NP_001243197.1:p.Pro894Ser
NM_032578.3:c.3562C>T , LRG_410t1:c.3562C>T	NP_115967.2:p.Pro1188Ser
NR_045662.3:n.2989C>T
NR_045663.3:n.3691C>T
XM_006718043.2:c.3616C>T	XP_006718106.1:p.Pro1206Ser
XM_011540292.1:c.3592C>T	XP_011538594.1:p.Pro1198Ser
XR_946029.1:n.1803+2134G>A
XM_017016833.1:c.3640C>T	XP_016872322.1:p.Pro1214Ser
XM_017016834.2:c.3562C>T	XP_016872323.1:p.Pro1188Ser
XM_024448236.1:c.2440C>T	XP_024304004.1:p.Pro814Ser
NR_045662.4:n.3099C>T
NR_045663.4:n.3636C>T
NM_001256267.2:c.3562C>T	NP_001243196.1:p.Pro1188Ser
NM_001256268.2:c.2680C>T	NP_001243197.1:p.Pro894Ser
NM_032578.4:c.3562C>T MANE Select	NP_115967.2:p.Pro1188Ser