Canonical Allele Identifier: CA376840961

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926387T>C (hg19) ; chr10:g.68166630T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166630T>C , CM000672.2:g.68166630T>C	GRCh38
NC_000010.10:g.69926387T>C , CM000672.1:g.69926387T>C	GRCh37
NC_000010.9:g.69596393T>C	NCBI36
NG_032118.1:g.65514T>C , LRG_410:g.65514T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1112T>C	ENSP00000346369.2:p.Val371Ala
ENST00000373675.4:c.1937T>C	ENSP00000362779.4:p.Val646Ala
ENST00000540630.6:c.1991T>C	ENSP00000441668.3:p.Val664Ala
ENST00000613327.5:c.1937T>C	ENSP00000480757.2:p.Val646Ala
ENST00000687572.1:c.815T>C	ENSP00000510427.1:p.Val272Ala
ENST00000688812.1:c.1913T>C	ENSP00000510658.1:p.Val638Ala
ENST00000690544.1:c.*1208T>C	ENSP00000508989.1:n.*1208T>C
ENST00000358913.10:c.1937T>C MANE Select	ENSP00000351790.5:p.Val646Ala
ENST00000354393.6:c.1112T>C	ENSP00000346369.2:p.Val371Ala
ENST00000358913.9:c.1937T>C	ENSP00000351790.5:p.Val646Ala
ENST00000540630.5:c.1937T>C	ENSP00000441668.2:p.Val646Ala
ENST00000613327.4:c.1055T>C	ENSP00000480757.1:p.Val352Ala
NM_001256267.1:c.1937T>C	NP_001243196.1:p.Val646Ala
NM_001256268.1:c.1055T>C	NP_001243197.1:p.Val352Ala
NM_032578.3:c.1937T>C , LRG_410t1:c.1937T>C	NP_115967.2:p.Val646Ala
NR_045662.3:n.1364T>C
NR_045663.3:n.2205T>C
XM_006718043.2:c.1991T>C	XP_006718106.1:p.Val664Ala
XM_011540292.1:c.1967T>C	XP_011538594.1:p.Val656Ala
XM_017016833.1:c.2015T>C	XP_016872322.1:p.Val672Ala
XM_017016834.2:c.1937T>C	XP_016872323.1:p.Val646Ala
XM_024448236.1:c.815T>C	XP_024304004.1:p.Val272Ala
NR_045662.4:n.1474T>C
NR_045663.4:n.2150T>C
NM_001256267.2:c.1937T>C	NP_001243196.1:p.Val646Ala
NM_001256268.2:c.1055T>C	NP_001243197.1:p.Val352Ala
NM_032578.4:c.1937T>C MANE Select	NP_115967.2:p.Val646Ala