Canonical Allele Identifier: CA376859269

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199494-C-T
• MyVariant Identifiers: chr10:g.69959251C>T (hg19) ; chr10:g.68199494C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199494C>T , CM000672.2:g.68199494C>T	GRCh38
NC_000010.10:g.69959251C>T , CM000672.1:g.69959251C>T	GRCh37
NC_000010.9:g.69629257C>T	NCBI36
NG_032118.1:g.98378C>T , LRG_410:g.98378C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2587C>T	ENSP00000346369.2:p.Gln863Ter
ENST00000540630.6:c.3466C>T	ENSP00000441668.3:p.Gln1156Ter
ENST00000613327.5:c.3412C>T	ENSP00000480757.2:p.Gln1138Ter
ENST00000688812.1:c.*675C>T	ENSP00000510658.1:n.*675C>T
ENST00000690544.1:c.*2683C>T	ENSP00000508989.1:n.*2683C>T
ENST00000358913.10:c.3412C>T MANE Select	ENSP00000351790.5:p.Gln1138Ter
ENST00000354393.6:c.2587C>T	ENSP00000346369.2:p.Gln863Ter
ENST00000358913.9:c.3412C>T	ENSP00000351790.5:p.Gln1138Ter
ENST00000540630.5:c.3412C>T	ENSP00000441668.2:p.Gln1138Ter
ENST00000613327.4:c.2530C>T	ENSP00000480757.1:p.Gln844Ter
NM_001256267.1:c.3412C>T	NP_001243196.1:p.Gln1138Ter
NM_001256268.1:c.2530C>T	NP_001243197.1:p.Gln844Ter
NM_032578.3:c.3412C>T , LRG_410t1:c.3412C>T	NP_115967.2:p.Gln1138Ter
NR_045662.3:n.2839C>T
NR_045663.3:n.3541C>T
XM_006718043.2:c.3466C>T	XP_006718106.1:p.Gln1156Ter
XM_011540292.1:c.3442C>T	XP_011538594.1:p.Gln1148Ter
XR_946029.1:n.1804-219G>A
XM_017016833.1:c.3490C>T	XP_016872322.1:p.Gln1164Ter
XM_017016834.2:c.3412C>T	XP_016872323.1:p.Gln1138Ter
XM_024448236.1:c.2290C>T	XP_024304004.1:p.Gln764Ter
NR_045662.4:n.2949C>T
NR_045663.4:n.3486C>T
NM_001256267.2:c.3412C>T	NP_001243196.1:p.Gln1138Ter
NM_001256268.2:c.2530C>T	NP_001243197.1:p.Gln844Ter
NM_032578.4:c.3412C>T MANE Select	NP_115967.2:p.Gln1138Ter