Canonical Allele Identifier: CA376859880

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69961603G>C (hg19) ; chr10:g.68201846G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68201846G>C , CM000672.2:g.68201846G>C	GRCh38
NC_000010.10:g.69961603G>C , CM000672.1:g.69961603G>C	GRCh37
NC_000010.9:g.69631609G>C	NCBI36
NG_032118.1:g.100730G>C , LRG_410:g.100730G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2686G>C	ENSP00000346369.2:p.Ala896Pro
ENST00000540630.6:c.3565G>C	ENSP00000441668.3:p.Ala1189Pro
ENST00000613327.5:c.3511G>C	ENSP00000480757.2:p.Ala1171Pro
ENST00000688812.1:c.*774G>C	ENSP00000510658.1:n.*774G>C
ENST00000690544.1:c.*2782G>C	ENSP00000508989.1:n.*2782G>C
ENST00000358913.10:c.3511G>C MANE Select	ENSP00000351790.5:p.Ala1171Pro
ENST00000354393.6:c.2686G>C	ENSP00000346369.2:p.Ala896Pro
ENST00000358913.9:c.3511G>C	ENSP00000351790.5:p.Ala1171Pro
ENST00000540630.5:c.3511G>C	ENSP00000441668.2:p.Ala1171Pro
ENST00000613327.4:c.2629G>C	ENSP00000480757.1:p.Ala877Pro
NM_001256267.1:c.3511G>C	NP_001243196.1:p.Ala1171Pro
NM_001256268.1:c.2629G>C	NP_001243197.1:p.Ala877Pro
NM_032578.3:c.3511G>C , LRG_410t1:c.3511G>C	NP_115967.2:p.Ala1171Pro
NR_045662.3:n.2938G>C
NR_045663.3:n.3640G>C
XM_006718043.2:c.3565G>C	XP_006718106.1:p.Ala1189Pro
XM_011540292.1:c.3541G>C	XP_011538594.1:p.Ala1181Pro
XR_946029.1:n.1803+2185C>G
XM_017016833.1:c.3589G>C	XP_016872322.1:p.Ala1197Pro
XM_017016834.2:c.3511G>C	XP_016872323.1:p.Ala1171Pro
XM_024448236.1:c.2389G>C	XP_024304004.1:p.Ala797Pro
NR_045662.4:n.3048G>C
NR_045663.4:n.3585G>C
NM_001256267.2:c.3511G>C	NP_001243196.1:p.Ala1171Pro
NM_001256268.2:c.2629G>C	NP_001243197.1:p.Ala877Pro
NM_032578.4:c.3511G>C MANE Select	NP_115967.2:p.Ala1171Pro