Canonical Allele Identifier: CA215307

Gene: MYPN

Linked Data

• ClinVar Variation Id: 31805
• ClinVar RCV Id: RCV000024498 ; RCV000214651 ; RCV000477347 ; RCV000254442
• dbSNP Id: rs71535754
• ExAC: 10:69926385 C / T
• gnomAD v2: 10-69926385-C-T
• gnomAD v3: 10-68166628-C-T
• gnomAD v4: 10-68166628-C-T
• MyVariant Identifiers: chr10:g.69926385C>T (hg19) ; chr10:g.68166628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166628C>T , CM000672.2:g.68166628C>T	GRCh38
NC_000010.10:g.69926385C>T , CM000672.1:g.69926385C>T	GRCh37
NC_000010.9:g.69596391C>T	NCBI36
NG_032118.1:g.65512C>T , LRG_410:g.65512C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1110C>T	ENSP00000346369.2:p.Pro370=
ENST00000373675.4:c.1935C>T	ENSP00000362779.4:p.Pro645=
ENST00000540630.6:c.1989C>T	ENSP00000441668.3:p.Pro663=
ENST00000613327.5:c.1935C>T	ENSP00000480757.2:p.Pro645=
ENST00000687572.1:c.813C>T	ENSP00000510427.1:p.Pro271=
ENST00000688812.1:c.1911C>T	ENSP00000510658.1:p.Pro637=
ENST00000690544.1:c.*1206C>T	ENSP00000508989.1:n.*1206C>T
ENST00000358913.10:c.1935C>T MANE Select	ENSP00000351790.5:p.Pro645=
ENST00000354393.6:c.1110C>T	ENSP00000346369.2:p.Pro370=
ENST00000358913.9:c.1935C>T	ENSP00000351790.5:p.Pro645=
ENST00000540630.5:c.1935C>T	ENSP00000441668.2:p.Pro645=
ENST00000613327.4:c.1053C>T	ENSP00000480757.1:p.Pro351=
NM_001256267.1:c.1935C>T	NP_001243196.1:p.Pro645=
NM_001256268.1:c.1053C>T	NP_001243197.1:p.Pro351=
NM_032578.3:c.1935C>T , LRG_410t1:c.1935C>T	NP_115967.2:p.Pro645=
NR_045662.3:n.1362C>T
NR_045663.3:n.2203C>T
XM_006718043.2:c.1989C>T	XP_006718106.1:p.Pro663=
XM_011540292.1:c.1965C>T	XP_011538594.1:p.Pro655=
XM_017016833.1:c.2013C>T	XP_016872322.1:p.Pro671=
XM_017016834.2:c.1935C>T	XP_016872323.1:p.Pro645=
XM_024448236.1:c.813C>T	XP_024304004.1:p.Pro271=
NR_045662.4:n.1472C>T
NR_045663.4:n.2148C>T
NM_001256267.2:c.1935C>T	NP_001243196.1:p.Pro645=
NM_001256268.2:c.1053C>T	NP_001243197.1:p.Pro351=
NM_032578.4:c.1935C>T MANE Select	NP_115967.2:p.Pro645=