Canonical Allele Identifier: CA469812215

Gene: MYPN

Linked Data

• gnomAD v4: 10-68197367-G-T
• MyVariant Identifiers: chr10:g.69957124G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197367G>T , CM000672.2:g.68197367G>T	GRCh38
NC_000010.10:g.69957124G>T , CM000672.1:g.69957124G>T	GRCh37
NC_000010.9:g.69627130G>T	NCBI36
NG_032118.1:g.96251G>T , LRG_410:g.96251G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2349G>T	ENSP00000346369.2:p.Val783=
ENST00000540630.6:c.3228G>T	ENSP00000441668.3:p.Val1076=
ENST00000613327.5:c.3174G>T	ENSP00000480757.2:p.Val1058=
ENST00000688812.1:c.*437G>T	ENSP00000510658.1:n.*437G>T
ENST00000690544.1:c.*2445G>T	ENSP00000508989.1:n.*2445G>T
ENST00000358913.10:c.3174G>T MANE Select	ENSP00000351790.5:p.Val1058=
ENST00000354393.6:c.2349G>T	ENSP00000346369.2:p.Val783=
ENST00000358913.9:c.3174G>T	ENSP00000351790.5:p.Val1058=
ENST00000540630.5:c.3174G>T	ENSP00000441668.2:p.Val1058=
ENST00000613327.4:c.2292G>T	ENSP00000480757.1:p.Val764=
NM_001256267.1:c.3174G>T	NP_001243196.1:p.Val1058=
NM_001256268.1:c.2292G>T	NP_001243197.1:p.Val764=
NM_032578.3:c.3174G>T , LRG_410t1:c.3174G>T	NP_115967.2:p.Val1058=
NR_045662.3:n.2601G>T
NR_045663.3:n.3303G>T
XM_006718043.2:c.3228G>T	XP_006718106.1:p.Val1076=
XM_011540292.1:c.3204G>T	XP_011538594.1:p.Val1068=
XM_017016833.1:c.3252G>T	XP_016872322.1:p.Val1084=
XM_017016834.2:c.3174G>T	XP_016872323.1:p.Val1058=
XM_024448236.1:c.2052G>T	XP_024304004.1:p.Val684=
NR_045662.4:n.2711G>T
NR_045663.4:n.3248G>T
NM_001256267.2:c.3174G>T	NP_001243196.1:p.Val1058=
NM_001256268.2:c.2292G>T	NP_001243197.1:p.Val764=
NM_032578.4:c.3174G>T MANE Select	NP_115967.2:p.Val1058=