Canonical Allele Identifier: CA376839433

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166324-T-C
• MyVariant Identifiers: chr10:g.69926081T>C (hg19) ; chr10:g.68166324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166324T>C , CM000672.2:g.68166324T>C	GRCh38
NC_000010.10:g.69926081T>C , CM000672.1:g.69926081T>C	GRCh37
NC_000010.9:g.69596087T>C	NCBI36
NG_032118.1:g.65208T>C , LRG_410:g.65208T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.806T>C	ENSP00000346369.2:p.Leu269Pro
ENST00000373675.4:c.1631T>C	ENSP00000362779.4:p.Leu544Pro
ENST00000540630.6:c.1685T>C	ENSP00000441668.3:p.Leu562Pro
ENST00000613327.5:c.1631T>C	ENSP00000480757.2:p.Leu544Pro
ENST00000687572.1:c.509T>C	ENSP00000510427.1:p.Leu170Pro
ENST00000687705.1:c.*1880T>C	ENSP00000509639.1:n.*1880T>C
ENST00000688812.1:c.1607T>C	ENSP00000510658.1:p.Leu536Pro
ENST00000689002.1:n.683T>C
ENST00000690544.1:c.*902T>C	ENSP00000508989.1:n.*902T>C
ENST00000358913.10:c.1631T>C MANE Select	ENSP00000351790.5:p.Leu544Pro
ENST00000354393.6:c.806T>C	ENSP00000346369.2:p.Leu269Pro
ENST00000358913.9:c.1631T>C	ENSP00000351790.5:p.Leu544Pro
ENST00000540630.5:c.1631T>C	ENSP00000441668.2:p.Leu544Pro
ENST00000613327.4:c.749T>C	ENSP00000480757.1:p.Leu250Pro
NM_001256267.1:c.1631T>C	NP_001243196.1:p.Leu544Pro
NM_001256268.1:c.749T>C	NP_001243197.1:p.Leu250Pro
NM_032578.3:c.1631T>C , LRG_410t1:c.1631T>C	NP_115967.2:p.Leu544Pro
NR_045662.3:n.1058T>C
NR_045663.3:n.1899T>C
XM_006718043.2:c.1685T>C	XP_006718106.1:p.Leu562Pro
XM_011540292.1:c.1661T>C	XP_011538594.1:p.Leu554Pro
XM_017016833.1:c.1709T>C	XP_016872322.1:p.Leu570Pro
XM_017016834.2:c.1631T>C	XP_016872323.1:p.Leu544Pro
XM_024448236.1:c.509T>C	XP_024304004.1:p.Leu170Pro
NR_045662.4:n.1168T>C
NR_045663.4:n.1844T>C
NM_001256267.2:c.1631T>C	NP_001243196.1:p.Leu544Pro
NM_001256268.2:c.749T>C	NP_001243197.1:p.Leu250Pro
NM_032578.4:c.1631T>C MANE Select	NP_115967.2:p.Leu544Pro