Canonical Allele Identifier: CA376840536

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926316G>T (hg19) ; chr10:g.68166559G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166559G>T , CM000672.2:g.68166559G>T	GRCh38
NC_000010.10:g.69926316G>T , CM000672.1:g.69926316G>T	GRCh37
NC_000010.9:g.69596322G>T	NCBI36
NG_032118.1:g.65443G>T , LRG_410:g.65443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1041G>T	ENSP00000346369.2:p.Gln347His
ENST00000373675.4:c.1866G>T	ENSP00000362779.4:p.Gln622His
ENST00000540630.6:c.1920G>T	ENSP00000441668.3:p.Gln640His
ENST00000613327.5:c.1866G>T	ENSP00000480757.2:p.Gln622His
ENST00000687572.1:c.744G>T	ENSP00000510427.1:p.Gln248His
ENST00000688812.1:c.1842G>T	ENSP00000510658.1:p.Gln614His
ENST00000690544.1:c.*1137G>T	ENSP00000508989.1:n.*1137G>T
ENST00000358913.10:c.1866G>T MANE Select	ENSP00000351790.5:p.Gln622His
ENST00000354393.6:c.1041G>T	ENSP00000346369.2:p.Gln347His
ENST00000358913.9:c.1866G>T	ENSP00000351790.5:p.Gln622His
ENST00000540630.5:c.1866G>T	ENSP00000441668.2:p.Gln622His
ENST00000613327.4:c.984G>T	ENSP00000480757.1:p.Gln328His
NM_001256267.1:c.1866G>T	NP_001243196.1:p.Gln622His
NM_001256268.1:c.984G>T	NP_001243197.1:p.Gln328His
NM_032578.3:c.1866G>T , LRG_410t1:c.1866G>T	NP_115967.2:p.Gln622His
NR_045662.3:n.1293G>T
NR_045663.3:n.2134G>T
XM_006718043.2:c.1920G>T	XP_006718106.1:p.Gln640His
XM_011540292.1:c.1896G>T	XP_011538594.1:p.Gln632His
XM_017016833.1:c.1944G>T	XP_016872322.1:p.Gln648His
XM_017016834.2:c.1866G>T	XP_016872323.1:p.Gln622His
XM_024448236.1:c.744G>T	XP_024304004.1:p.Gln248His
NR_045662.4:n.1403G>T
NR_045663.4:n.2079G>T
NM_001256267.2:c.1866G>T	NP_001243196.1:p.Gln622His
NM_001256268.2:c.984G>T	NP_001243197.1:p.Gln328His
NM_032578.4:c.1866G>T MANE Select	NP_115967.2:p.Gln622His