Canonical Allele Identifier: CA208222869

Gene: MYPN

Linked Data

• dbSNP Id: rs770562444
• gnomAD v3: 10-68195519-G-A
• gnomAD v4: 10-68195519-G-A
• MyVariant Identifiers: chr10:g.69955276G>A (hg19) ; chr10:g.68195519G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195519G>A , CM000672.2:g.68195519G>A	GRCh38
NC_000010.10:g.69955276G>A , CM000672.1:g.69955276G>A	GRCh37
NC_000010.9:g.69625282G>A	NCBI36
NG_032118.1:g.94403G>A , LRG_410:g.94403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2320G>A	ENSP00000346369.2:p.Gly774Ser
ENST00000540630.6:c.3199G>A	ENSP00000441668.3:p.Gly1067Ser
ENST00000613327.5:c.3145G>A	ENSP00000480757.2:p.Gly1049Ser
ENST00000688812.1:c.*408G>A	ENSP00000510658.1:n.*408G>A
ENST00000690544.1:c.*2416G>A	ENSP00000508989.1:n.*2416G>A
ENST00000358913.10:c.3145G>A MANE Select	ENSP00000351790.5:p.Gly1049Ser
ENST00000354393.6:c.2320G>A	ENSP00000346369.2:p.Gly774Ser
ENST00000358913.9:c.3145G>A	ENSP00000351790.5:p.Gly1049Ser
ENST00000540630.5:c.3145G>A	ENSP00000441668.2:p.Gly1049Ser
ENST00000613327.4:c.2263G>A	ENSP00000480757.1:p.Gly755Ser
NM_001256267.1:c.3145G>A	NP_001243196.1:p.Gly1049Ser
NM_001256268.1:c.2263G>A	NP_001243197.1:p.Gly755Ser
NM_032578.3:c.3145G>A , LRG_410t1:c.3145G>A	NP_115967.2:p.Gly1049Ser
NR_045662.3:n.2572G>A
NR_045663.3:n.3274G>A
XM_006718043.2:c.3199G>A	XP_006718106.1:p.Gly1067Ser
XM_011540292.1:c.3175G>A	XP_011538594.1:p.Gly1059Ser
XM_017016833.1:c.3223G>A	XP_016872322.1:p.Gly1075Ser
XM_017016834.2:c.3145G>A	XP_016872323.1:p.Gly1049Ser
XM_024448236.1:c.2023G>A	XP_024304004.1:p.Gly675Ser
NR_045662.4:n.2682G>A
NR_045663.4:n.3219G>A
NM_001256267.2:c.3145G>A	NP_001243196.1:p.Gly1049Ser
NM_001256268.2:c.2263G>A	NP_001243197.1:p.Gly755Ser
NM_032578.4:c.3145G>A MANE Select	NP_115967.2:p.Gly1049Ser