Canonical Allele Identifier: CA391381235

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386654T>A (hg19) ; chr15:g.28141508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141508T>A , CM000677.2:g.28141508T>A	GRCh38
NC_000015.9:g.28386654T>A , CM000677.1:g.28386654T>A	GRCh37
NC_000015.8:g.26060249T>A	NCBI36
NG_016355.1:g.185642A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11939A>T MANE Select	ENSP00000261609.8:p.Glu3980Val
ENST00000650509.1:c.3650A>T	ENSP00000496936.1:p.Glu1217Val
ENST00000261609.11:c.11939A>T	ENSP00000261609.7:p.Glu3980Val
NM_004667.5:c.11939A>T	NP_004658.3:p.Glu3980Val
XM_005268276.3:c.11825A>T	XP_005268333.1:p.Glu3942Val
XM_005268277.3:c.11825A>T	XP_005268334.1:p.Glu3942Val
XM_006720726.2:c.11924A>T	XP_006720789.1:p.Glu3975Val
XM_006720727.2:c.11681A>T	XP_006720790.1:p.Glu3894Val
XM_011522131.1:c.11456A>T	XP_011520433.1:p.Glu3819Val
XM_011522132.1:c.9455A>T	XP_011520434.1:p.Glu3152Val
XM_011522133.1:c.8684A>T	XP_011520435.1:p.Glu2895Val
XM_011522134.1:c.6056A>T	XP_011520436.1:p.Glu2019Val
XM_005268276.5:c.11825A>T	XP_005268333.1:p.Glu3942Val
XM_006720726.3:c.11924A>T	XP_006720789.1:p.Glu3975Val
XM_006720727.3:c.11681A>T	XP_006720790.1:p.Glu3894Val
XM_017022695.1:c.11825A>T	XP_016878184.1:p.Glu3942Val
XM_017022696.1:c.11825A>T	XP_016878185.1:p.Glu3942Val
XM_017022697.1:c.5105A>T	XP_016878186.1:p.Glu1702Val
XM_017022698.1:c.5105A>T	XP_016878187.1:p.Glu1702Val
NM_004667.6:c.11939A>T MANE Select	NP_004658.3:p.Glu3980Val