Canonical Allele Identifier: CA376857761

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69955282T>C (hg19) ; chr10:g.68195525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195525T>C , CM000672.2:g.68195525T>C	GRCh38
NC_000010.10:g.69955282T>C , CM000672.1:g.69955282T>C	GRCh37
NC_000010.9:g.69625288T>C	NCBI36
NG_032118.1:g.94409T>C , LRG_410:g.94409T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2326T>C	ENSP00000346369.2:p.Ser776Pro
ENST00000540630.6:c.3205T>C	ENSP00000441668.3:p.Ser1069Pro
ENST00000613327.5:c.3151T>C	ENSP00000480757.2:p.Ser1051Pro
ENST00000688812.1:c.*414T>C	ENSP00000510658.1:n.*414T>C
ENST00000690544.1:c.*2422T>C	ENSP00000508989.1:n.*2422T>C
ENST00000358913.10:c.3151T>C MANE Select	ENSP00000351790.5:p.Ser1051Pro
ENST00000354393.6:c.2326T>C	ENSP00000346369.2:p.Ser776Pro
ENST00000358913.9:c.3151T>C	ENSP00000351790.5:p.Ser1051Pro
ENST00000540630.5:c.3151T>C	ENSP00000441668.2:p.Ser1051Pro
ENST00000613327.4:c.2269T>C	ENSP00000480757.1:p.Ser757Pro
NM_001256267.1:c.3151T>C	NP_001243196.1:p.Ser1051Pro
NM_001256268.1:c.2269T>C	NP_001243197.1:p.Ser757Pro
NM_032578.3:c.3151T>C , LRG_410t1:c.3151T>C	NP_115967.2:p.Ser1051Pro
NR_045662.3:n.2578T>C
NR_045663.3:n.3280T>C
XM_006718043.2:c.3205T>C	XP_006718106.1:p.Ser1069Pro
XM_011540292.1:c.3181T>C	XP_011538594.1:p.Ser1061Pro
XM_017016833.1:c.3229T>C	XP_016872322.1:p.Ser1077Pro
XM_017016834.2:c.3151T>C	XP_016872323.1:p.Ser1051Pro
XM_024448236.1:c.2029T>C	XP_024304004.1:p.Ser677Pro
NR_045662.4:n.2688T>C
NR_045663.4:n.3225T>C
NM_001256267.2:c.3151T>C	NP_001243196.1:p.Ser1051Pro
NM_001256268.2:c.2269T>C	NP_001243197.1:p.Ser757Pro
NM_032578.4:c.3151T>C MANE Select	NP_115967.2:p.Ser1051Pro