Canonical Allele Identifier: CA376857320

Gene: MYPN

Linked Data

• gnomAD v4: 10-68195463-G-A
• MyVariant Identifiers: chr10:g.69955220G>A (hg19) ; chr10:g.68195463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195463G>A , CM000672.2:g.68195463G>A	GRCh38
NC_000010.10:g.69955220G>A , CM000672.1:g.69955220G>A	GRCh37
NC_000010.9:g.69625226G>A	NCBI36
NG_032118.1:g.94347G>A , LRG_410:g.94347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2264G>A	ENSP00000346369.2:p.Cys755Tyr
ENST00000540630.6:c.3143G>A	ENSP00000441668.3:p.Cys1048Tyr
ENST00000613327.5:c.3089G>A	ENSP00000480757.2:p.Cys1030Tyr
ENST00000688812.1:c.*352G>A	ENSP00000510658.1:n.*352G>A
ENST00000690544.1:c.*2360G>A	ENSP00000508989.1:n.*2360G>A
ENST00000358913.10:c.3089G>A MANE Select	ENSP00000351790.5:p.Cys1030Tyr
ENST00000354393.6:c.2264G>A	ENSP00000346369.2:p.Cys755Tyr
ENST00000358913.9:c.3089G>A	ENSP00000351790.5:p.Cys1030Tyr
ENST00000540630.5:c.3089G>A	ENSP00000441668.2:p.Cys1030Tyr
ENST00000613327.4:c.2207G>A	ENSP00000480757.1:p.Cys736Tyr
NM_001256267.1:c.3089G>A	NP_001243196.1:p.Cys1030Tyr
NM_001256268.1:c.2207G>A	NP_001243197.1:p.Cys736Tyr
NM_032578.3:c.3089G>A , LRG_410t1:c.3089G>A	NP_115967.2:p.Cys1030Tyr
NR_045662.3:n.2516G>A
NR_045663.3:n.3218G>A
XM_006718043.2:c.3143G>A	XP_006718106.1:p.Cys1048Tyr
XM_011540292.1:c.3119G>A	XP_011538594.1:p.Cys1040Tyr
XM_017016833.1:c.3167G>A	XP_016872322.1:p.Cys1056Tyr
XM_017016834.2:c.3089G>A	XP_016872323.1:p.Cys1030Tyr
XM_024448236.1:c.1967G>A	XP_024304004.1:p.Cys656Tyr
NR_045662.4:n.2626G>A
NR_045663.4:n.3163G>A
NM_001256267.2:c.3089G>A	NP_001243196.1:p.Cys1030Tyr
NM_001256268.2:c.2207G>A	NP_001243197.1:p.Cys736Tyr
NM_032578.4:c.3089G>A MANE Select	NP_115967.2:p.Cys1030Tyr