Canonical Allele Identifier: CA376858888

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959135T>C (hg19) ; chr10:g.68199378T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199378T>C , CM000672.2:g.68199378T>C	GRCh38
NC_000010.10:g.69959135T>C , CM000672.1:g.69959135T>C	GRCh37
NC_000010.9:g.69629141T>C	NCBI36
NG_032118.1:g.98262T>C , LRG_410:g.98262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2471T>C	ENSP00000346369.2:p.Leu824Ser
ENST00000540630.6:c.3350T>C	ENSP00000441668.3:p.Leu1117Ser
ENST00000613327.5:c.3296T>C	ENSP00000480757.2:p.Leu1099Ser
ENST00000688812.1:c.*559T>C	ENSP00000510658.1:n.*559T>C
ENST00000690544.1:c.*2567T>C	ENSP00000508989.1:n.*2567T>C
ENST00000358913.10:c.3296T>C MANE Select	ENSP00000351790.5:p.Leu1099Ser
ENST00000354393.6:c.2471T>C	ENSP00000346369.2:p.Leu824Ser
ENST00000358913.9:c.3296T>C	ENSP00000351790.5:p.Leu1099Ser
ENST00000540630.5:c.3296T>C	ENSP00000441668.2:p.Leu1099Ser
ENST00000613327.4:c.2414T>C	ENSP00000480757.1:p.Leu805Ser
NM_001256267.1:c.3296T>C	NP_001243196.1:p.Leu1099Ser
NM_001256268.1:c.2414T>C	NP_001243197.1:p.Leu805Ser
NM_032578.3:c.3296T>C , LRG_410t1:c.3296T>C	NP_115967.2:p.Leu1099Ser
NR_045662.3:n.2723T>C
NR_045663.3:n.3425T>C
XM_006718043.2:c.3350T>C	XP_006718106.1:p.Leu1117Ser
XM_011540292.1:c.3326T>C	XP_011538594.1:p.Leu1109Ser
XR_946029.1:n.1804-103A>G
XM_017016833.1:c.3374T>C	XP_016872322.1:p.Leu1125Ser
XM_017016834.2:c.3296T>C	XP_016872323.1:p.Leu1099Ser
XM_024448236.1:c.2174T>C	XP_024304004.1:p.Leu725Ser
NR_045662.4:n.2833T>C
NR_045663.4:n.3370T>C
NM_001256267.2:c.3296T>C	NP_001243196.1:p.Leu1099Ser
NM_001256268.2:c.2414T>C	NP_001243197.1:p.Leu805Ser
NM_032578.4:c.3296T>C MANE Select	NP_115967.2:p.Leu1099Ser