Canonical Allele Identifier: CA469813010

Gene: MYPN

Linked Data

• gnomAD v4: 10-68166562-C-T
• MyVariant Identifiers: chr10:g.69926319C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166562C>T , CM000672.2:g.68166562C>T	GRCh38
NC_000010.10:g.69926319C>T , CM000672.1:g.69926319C>T	GRCh37
NC_000010.9:g.69596325C>T	NCBI36
NG_032118.1:g.65446C>T , LRG_410:g.65446C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1044C>T	ENSP00000346369.2:p.Thr348=
ENST00000373675.4:c.1869C>T	ENSP00000362779.4:p.Thr623=
ENST00000540630.6:c.1923C>T	ENSP00000441668.3:p.Thr641=
ENST00000613327.5:c.1869C>T	ENSP00000480757.2:p.Thr623=
ENST00000687572.1:c.747C>T	ENSP00000510427.1:p.Thr249=
ENST00000688812.1:c.1845C>T	ENSP00000510658.1:p.Thr615=
ENST00000690544.1:c.*1140C>T	ENSP00000508989.1:n.*1140C>T
ENST00000358913.10:c.1869C>T MANE Select	ENSP00000351790.5:p.Thr623=
ENST00000354393.6:c.1044C>T	ENSP00000346369.2:p.Thr348=
ENST00000358913.9:c.1869C>T	ENSP00000351790.5:p.Thr623=
ENST00000540630.5:c.1869C>T	ENSP00000441668.2:p.Thr623=
ENST00000613327.4:c.987C>T	ENSP00000480757.1:p.Thr329=
NM_001256267.1:c.1869C>T	NP_001243196.1:p.Thr623=
NM_001256268.1:c.987C>T	NP_001243197.1:p.Thr329=
NM_032578.3:c.1869C>T , LRG_410t1:c.1869C>T	NP_115967.2:p.Thr623=
NR_045662.3:n.1296C>T
NR_045663.3:n.2137C>T
XM_006718043.2:c.1923C>T	XP_006718106.1:p.Thr641=
XM_011540292.1:c.1899C>T	XP_011538594.1:p.Thr633=
XM_017016833.1:c.1947C>T	XP_016872322.1:p.Thr649=
XM_017016834.2:c.1869C>T	XP_016872323.1:p.Thr623=
XM_024448236.1:c.747C>T	XP_024304004.1:p.Thr249=
NR_045662.4:n.1406C>T
NR_045663.4:n.2082C>T
NM_001256267.2:c.1869C>T	NP_001243196.1:p.Thr623=
NM_001256268.2:c.987C>T	NP_001243197.1:p.Thr329=
NM_032578.4:c.1869C>T MANE Select	NP_115967.2:p.Thr623=