Canonical Allele Identifier: CA376859200

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199468-A-C
• MyVariant Identifiers: chr10:g.69959225A>C (hg19) ; chr10:g.68199468A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199468A>C , CM000672.2:g.68199468A>C	GRCh38
NC_000010.10:g.69959225A>C , CM000672.1:g.69959225A>C	GRCh37
NC_000010.9:g.69629231A>C	NCBI36
NG_032118.1:g.98352A>C , LRG_410:g.98352A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2561A>C	ENSP00000346369.2:p.His854Pro
ENST00000540630.6:c.3440A>C	ENSP00000441668.3:p.His1147Pro
ENST00000613327.5:c.3386A>C	ENSP00000480757.2:p.His1129Pro
ENST00000688812.1:c.*649A>C	ENSP00000510658.1:n.*649A>C
ENST00000690544.1:c.*2657A>C	ENSP00000508989.1:n.*2657A>C
ENST00000358913.10:c.3386A>C MANE Select	ENSP00000351790.5:p.His1129Pro
ENST00000354393.6:c.2561A>C	ENSP00000346369.2:p.His854Pro
ENST00000358913.9:c.3386A>C	ENSP00000351790.5:p.His1129Pro
ENST00000540630.5:c.3386A>C	ENSP00000441668.2:p.His1129Pro
ENST00000613327.4:c.2504A>C	ENSP00000480757.1:p.His835Pro
NM_001256267.1:c.3386A>C	NP_001243196.1:p.His1129Pro
NM_001256268.1:c.2504A>C	NP_001243197.1:p.His835Pro
NM_032578.3:c.3386A>C , LRG_410t1:c.3386A>C	NP_115967.2:p.His1129Pro
NR_045662.3:n.2813A>C
NR_045663.3:n.3515A>C
XM_006718043.2:c.3440A>C	XP_006718106.1:p.His1147Pro
XM_011540292.1:c.3416A>C	XP_011538594.1:p.His1139Pro
XR_946029.1:n.1804-193T>G
XM_017016833.1:c.3464A>C	XP_016872322.1:p.His1155Pro
XM_017016834.2:c.3386A>C	XP_016872323.1:p.His1129Pro
XM_024448236.1:c.2264A>C	XP_024304004.1:p.His755Pro
NR_045662.4:n.2923A>C
NR_045663.4:n.3460A>C
NM_001256267.2:c.3386A>C	NP_001243196.1:p.His1129Pro
NM_001256268.2:c.2504A>C	NP_001243197.1:p.His835Pro
NM_032578.4:c.3386A>C MANE Select	NP_115967.2:p.His1129Pro