Canonical Allele Identifier: CA376857437

Gene: MYPN

Linked Data

• ClinVar Variation Id: 544042
• ClinVar RCV Id: RCV000655047
• dbSNP Id: rs1554850184
• MyVariant Identifiers: chr10:g.69955238T>C (hg19) ; chr10:g.68195481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195481T>C , CM000672.2:g.68195481T>C	GRCh38
NC_000010.10:g.69955238T>C , CM000672.1:g.69955238T>C	GRCh37
NC_000010.9:g.69625244T>C	NCBI36
NG_032118.1:g.94365T>C , LRG_410:g.94365T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2282T>C	ENSP00000346369.2:p.Val761Ala
ENST00000540630.6:c.3161T>C	ENSP00000441668.3:p.Val1054Ala
ENST00000613327.5:c.3107T>C	ENSP00000480757.2:p.Val1036Ala
ENST00000688812.1:c.*370T>C	ENSP00000510658.1:n.*370T>C
ENST00000690544.1:c.*2378T>C	ENSP00000508989.1:n.*2378T>C
ENST00000358913.10:c.3107T>C MANE Select	ENSP00000351790.5:p.Val1036Ala
ENST00000354393.6:c.2282T>C	ENSP00000346369.2:p.Val761Ala
ENST00000358913.9:c.3107T>C	ENSP00000351790.5:p.Val1036Ala
ENST00000540630.5:c.3107T>C	ENSP00000441668.2:p.Val1036Ala
ENST00000613327.4:c.2225T>C	ENSP00000480757.1:p.Val742Ala
NM_001256267.1:c.3107T>C	NP_001243196.1:p.Val1036Ala
NM_001256268.1:c.2225T>C	NP_001243197.1:p.Val742Ala
NM_032578.3:c.3107T>C , LRG_410t1:c.3107T>C	NP_115967.2:p.Val1036Ala
NR_045662.3:n.2534T>C
NR_045663.3:n.3236T>C
XM_006718043.2:c.3161T>C	XP_006718106.1:p.Val1054Ala
XM_011540292.1:c.3137T>C	XP_011538594.1:p.Val1046Ala
XM_017016833.1:c.3185T>C	XP_016872322.1:p.Val1062Ala
XM_017016834.2:c.3107T>C	XP_016872323.1:p.Val1036Ala
XM_024448236.1:c.1985T>C	XP_024304004.1:p.Val662Ala
NR_045662.4:n.2644T>C
NR_045663.4:n.3181T>C
NM_001256267.2:c.3107T>C	NP_001243196.1:p.Val1036Ala
NM_001256268.2:c.2225T>C	NP_001243197.1:p.Val742Ala
NM_032578.4:c.3107T>C MANE Select	NP_115967.2:p.Val1036Ala