Canonical Allele Identifier: CA376859266

Gene: MYPN

Linked Data

• dbSNP Id: rs1317590648
• gnomAD v3: 10-68199492-C-T
• gnomAD v4: 10-68199492-C-T
• MyVariant Identifiers: chr10:g.69959249C>T (hg19) ; chr10:g.68199492C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199492C>T , CM000672.2:g.68199492C>T	GRCh38
NC_000010.10:g.69959249C>T , CM000672.1:g.69959249C>T	GRCh37
NC_000010.9:g.69629255C>T	NCBI36
NG_032118.1:g.98376C>T , LRG_410:g.98376C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2585C>T	ENSP00000346369.2:p.Thr862Ile
ENST00000540630.6:c.3464C>T	ENSP00000441668.3:p.Thr1155Ile
ENST00000613327.5:c.3410C>T	ENSP00000480757.2:p.Thr1137Ile
ENST00000688812.1:c.*673C>T	ENSP00000510658.1:n.*673C>T
ENST00000690544.1:c.*2681C>T	ENSP00000508989.1:n.*2681C>T
ENST00000358913.10:c.3410C>T MANE Select	ENSP00000351790.5:p.Thr1137Ile
ENST00000354393.6:c.2585C>T	ENSP00000346369.2:p.Thr862Ile
ENST00000358913.9:c.3410C>T	ENSP00000351790.5:p.Thr1137Ile
ENST00000540630.5:c.3410C>T	ENSP00000441668.2:p.Thr1137Ile
ENST00000613327.4:c.2528C>T	ENSP00000480757.1:p.Thr843Ile
NM_001256267.1:c.3410C>T	NP_001243196.1:p.Thr1137Ile
NM_001256268.1:c.2528C>T	NP_001243197.1:p.Thr843Ile
NM_032578.3:c.3410C>T , LRG_410t1:c.3410C>T	NP_115967.2:p.Thr1137Ile
NR_045662.3:n.2837C>T
NR_045663.3:n.3539C>T
XM_006718043.2:c.3464C>T	XP_006718106.1:p.Thr1155Ile
XM_011540292.1:c.3440C>T	XP_011538594.1:p.Thr1147Ile
XR_946029.1:n.1804-217G>A
XM_017016833.1:c.3488C>T	XP_016872322.1:p.Thr1163Ile
XM_017016834.2:c.3410C>T	XP_016872323.1:p.Thr1137Ile
XM_024448236.1:c.2288C>T	XP_024304004.1:p.Thr763Ile
NR_045662.4:n.2947C>T
NR_045663.4:n.3484C>T
NM_001256267.2:c.3410C>T	NP_001243196.1:p.Thr1137Ile
NM_001256268.2:c.2528C>T	NP_001243197.1:p.Thr843Ile
NM_032578.4:c.3410C>T MANE Select	NP_115967.2:p.Thr1137Ile