Canonical Allele Identifier: CA376858879

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959132G>C (hg19) ; chr10:g.68199375G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199375G>C , CM000672.2:g.68199375G>C	GRCh38
NC_000010.10:g.69959132G>C , CM000672.1:g.69959132G>C	GRCh37
NC_000010.9:g.69629138G>C	NCBI36
NG_032118.1:g.98259G>C , LRG_410:g.98259G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2468G>C	ENSP00000346369.2:p.Gly823Ala
ENST00000540630.6:c.3347G>C	ENSP00000441668.3:p.Gly1116Ala
ENST00000613327.5:c.3293G>C	ENSP00000480757.2:p.Gly1098Ala
ENST00000688812.1:c.*556G>C	ENSP00000510658.1:n.*556G>C
ENST00000690544.1:c.*2564G>C	ENSP00000508989.1:n.*2564G>C
ENST00000358913.10:c.3293G>C MANE Select	ENSP00000351790.5:p.Gly1098Ala
ENST00000354393.6:c.2468G>C	ENSP00000346369.2:p.Gly823Ala
ENST00000358913.9:c.3293G>C	ENSP00000351790.5:p.Gly1098Ala
ENST00000540630.5:c.3293G>C	ENSP00000441668.2:p.Gly1098Ala
ENST00000613327.4:c.2411G>C	ENSP00000480757.1:p.Gly804Ala
NM_001256267.1:c.3293G>C	NP_001243196.1:p.Gly1098Ala
NM_001256268.1:c.2411G>C	NP_001243197.1:p.Gly804Ala
NM_032578.3:c.3293G>C , LRG_410t1:c.3293G>C	NP_115967.2:p.Gly1098Ala
NR_045662.3:n.2720G>C
NR_045663.3:n.3422G>C
XM_006718043.2:c.3347G>C	XP_006718106.1:p.Gly1116Ala
XM_011540292.1:c.3323G>C	XP_011538594.1:p.Gly1108Ala
XR_946029.1:n.1804-100C>G
XM_017016833.1:c.3371G>C	XP_016872322.1:p.Gly1124Ala
XM_017016834.2:c.3293G>C	XP_016872323.1:p.Gly1098Ala
XM_024448236.1:c.2171G>C	XP_024304004.1:p.Gly724Ala
NR_045662.4:n.2830G>C
NR_045663.4:n.3367G>C
NM_001256267.2:c.3293G>C	NP_001243196.1:p.Gly1098Ala
NM_001256268.2:c.2411G>C	NP_001243197.1:p.Gly804Ala
NM_032578.4:c.3293G>C MANE Select	NP_115967.2:p.Gly1098Ala