Canonical Allele Identifier: CA391381934

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386935C>A (hg19) ; chr15:g.28141789C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141789C>A , CM000677.2:g.28141789C>A	GRCh38
NC_000015.9:g.28386935C>A , CM000677.1:g.28386935C>A	GRCh37
NC_000015.8:g.26060530C>A	NCBI36
NG_016355.1:g.185361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11758G>T MANE Select	ENSP00000261609.8:p.Glu3920Ter
ENST00000650509.1:c.3469G>T	ENSP00000496936.1:p.Glu1157Ter
ENST00000261609.11:c.11758G>T	ENSP00000261609.7:p.Glu3920Ter
ENST00000564519.1:n.273G>T
NM_004667.5:c.11758G>T	NP_004658.3:p.Glu3920Ter
XM_005268276.3:c.11644G>T	XP_005268333.1:p.Glu3882Ter
XM_005268277.3:c.11644G>T	XP_005268334.1:p.Glu3882Ter
XM_006720726.2:c.11743G>T	XP_006720789.1:p.Glu3915Ter
XM_006720727.2:c.11500G>T	XP_006720790.1:p.Glu3834Ter
XM_011522131.1:c.11275G>T	XP_011520433.1:p.Glu3759Ter
XM_011522132.1:c.9274G>T	XP_011520434.1:p.Glu3092Ter
XM_011522133.1:c.8503G>T	XP_011520435.1:p.Glu2835Ter
XM_011522134.1:c.5875G>T	XP_011520436.1:p.Glu1959Ter
XM_005268276.5:c.11644G>T	XP_005268333.1:p.Glu3882Ter
XM_006720726.3:c.11743G>T	XP_006720789.1:p.Glu3915Ter
XM_006720727.3:c.11500G>T	XP_006720790.1:p.Glu3834Ter
XM_017022695.1:c.11644G>T	XP_016878184.1:p.Glu3882Ter
XM_017022696.1:c.11644G>T	XP_016878185.1:p.Glu3882Ter
XM_017022697.1:c.4924G>T	XP_016878186.1:p.Glu1642Ter
XM_017022698.1:c.4924G>T	XP_016878187.1:p.Glu1642Ter
NM_004667.6:c.11758G>T MANE Select	NP_004658.3:p.Glu3920Ter