Canonical Allele Identifier: CA377105085

Gene: MYPN

Linked Data

• ClinVar Variation Id: 3228180
• ClinVar RCV Id: RCV004519890
• MyVariant Identifiers: chr10:g.69881971T>C (hg19) ; chr10:g.68122214T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68122214T>C , CM000672.2:g.68122214T>C	GRCh38
NC_000010.10:g.69881971T>C , CM000672.1:g.69881971T>C	GRCh37
NC_000010.9:g.69551977T>C	NCBI36
NG_032118.1:g.21098T>C , LRG_410:g.21098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.77+15413T>C	ENSP00000346369.2:n.77+15413T>C
ENST00000373675.4:c.776T>C	ENSP00000362779.4:p.Leu259Pro
ENST00000540630.6:c.776T>C	ENSP00000441668.3:p.Leu259Pro
ENST00000613327.5:c.776T>C	ENSP00000480757.2:p.Leu259Pro
ENST00000685006.1:c.848T>C	ENSP00000510318.1:p.Leu283Pro
ENST00000685060.1:n.1013T>C
ENST00000685154.1:c.776T>C	ENSP00000509251.1:p.Leu259Pro
ENST00000685627.1:c.*787T>C	ENSP00000508637.1:n.*787T>C
ENST00000686289.1:n.113+16031T>C
ENST00000687572.1:c.-221+16031T>C	ENSP00000510427.1:n.-221+16031T>C
ENST00000687705.1:c.*1025T>C	ENSP00000509639.1:n.*1025T>C
ENST00000688812.1:c.776T>C	ENSP00000510658.1:p.Leu259Pro
ENST00000689218.1:n.1005T>C
ENST00000689484.1:c.-220-20726T>C	ENSP00000509884.1:n.-220-20726T>C
ENST00000689797.1:c.-220-20726T>C	ENSP00000510689.1:n.-220-20726T>C
ENST00000690544.1:c.776T>C	ENSP00000508989.1:p.Leu259Pro
ENST00000692038.1:c.*1025T>C	ENSP00000509220.1:n.*1025T>C
ENST00000692953.1:n.62+16031T>C
ENST00000692979.1:c.776T>C	ENSP00000509849.1:p.Leu259Pro
ENST00000358913.10:c.776T>C MANE Select	ENSP00000351790.5:p.Leu259Pro
ENST00000354393.6:c.77+15413T>C	ENSP00000346369.2:n.77+15413T>C
ENST00000358913.9:c.776T>C	ENSP00000351790.5:p.Leu259Pro
ENST00000373675.3:c.776T>C	ENSP00000362779.3:p.Leu259Pro
ENST00000540630.5:c.776T>C	ENSP00000441668.2:p.Leu259Pro
ENST00000613327.4:c.-347T>C	ENSP00000480757.1:n.-347T>C
NM_001256267.1:c.776T>C	NP_001243196.1:p.Leu259Pro
NM_001256268.1:c.-347T>C	NP_001243197.1:n.-347T>C
NM_032578.3:c.776T>C , LRG_410t1:c.776T>C	NP_115967.2:p.Leu259Pro
NR_045662.3:n.329+15413T>C
NR_045663.3:n.1068T>C
XM_006718043.2:c.776T>C	XP_006718106.1:p.Leu259Pro
XM_011540292.1:c.776T>C	XP_011538594.1:p.Leu259Pro
XM_017016833.1:c.854T>C	XP_016872322.1:p.Leu285Pro
XM_017016834.2:c.776T>C	XP_016872323.1:p.Leu259Pro
XM_024448236.1:c.-221+16031T>C	XP_024304004.1:n.-221+16031T>C
NR_045662.4:n.439+15413T>C
NR_045663.4:n.1013T>C
NM_001256267.2:c.776T>C	NP_001243196.1:p.Leu259Pro
NM_001256268.2:c.-347T>C	NP_001243197.1:n.-347T>C
NM_032578.4:c.776T>C MANE Select	NP_115967.2:p.Leu259Pro