Canonical Allele Identifier: CA376840813

Gene: MYPN

Linked Data

• dbSNP Id: rs754801649
• gnomAD v2: 10-69926365-A-C
• MyVariant Identifiers: chr10:g.69926365A>C (hg19) ; chr10:g.68166608A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166608A>C , CM000672.2:g.68166608A>C	GRCh38
NC_000010.10:g.69926365A>C , CM000672.1:g.69926365A>C	GRCh37
NC_000010.9:g.69596371A>C	NCBI36
NG_032118.1:g.65492A>C , LRG_410:g.65492A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1090A>C	ENSP00000346369.2:p.Thr364Pro
ENST00000373675.4:c.1915A>C	ENSP00000362779.4:p.Thr639Pro
ENST00000540630.6:c.1969A>C	ENSP00000441668.3:p.Thr657Pro
ENST00000613327.5:c.1915A>C	ENSP00000480757.2:p.Thr639Pro
ENST00000687572.1:c.793A>C	ENSP00000510427.1:p.Thr265Pro
ENST00000688812.1:c.1891A>C	ENSP00000510658.1:p.Thr631Pro
ENST00000690544.1:c.*1186A>C	ENSP00000508989.1:n.*1186A>C
ENST00000358913.10:c.1915A>C MANE Select	ENSP00000351790.5:p.Thr639Pro
ENST00000354393.6:c.1090A>C	ENSP00000346369.2:p.Thr364Pro
ENST00000358913.9:c.1915A>C	ENSP00000351790.5:p.Thr639Pro
ENST00000540630.5:c.1915A>C	ENSP00000441668.2:p.Thr639Pro
ENST00000613327.4:c.1033A>C	ENSP00000480757.1:p.Thr345Pro
NM_001256267.1:c.1915A>C	NP_001243196.1:p.Thr639Pro
NM_001256268.1:c.1033A>C	NP_001243197.1:p.Thr345Pro
NM_032578.3:c.1915A>C , LRG_410t1:c.1915A>C	NP_115967.2:p.Thr639Pro
NR_045662.3:n.1342A>C
NR_045663.3:n.2183A>C
XM_006718043.2:c.1969A>C	XP_006718106.1:p.Thr657Pro
XM_011540292.1:c.1945A>C	XP_011538594.1:p.Thr649Pro
XM_017016833.1:c.1993A>C	XP_016872322.1:p.Thr665Pro
XM_017016834.2:c.1915A>C	XP_016872323.1:p.Thr639Pro
XM_024448236.1:c.793A>C	XP_024304004.1:p.Thr265Pro
NR_045662.4:n.1452A>C
NR_045663.4:n.2128A>C
NM_001256267.2:c.1915A>C	NP_001243196.1:p.Thr639Pro
NM_001256268.2:c.1033A>C	NP_001243197.1:p.Thr345Pro
NM_032578.4:c.1915A>C MANE Select	NP_115967.2:p.Thr639Pro