Canonical Allele Identifier: CA489234768

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386692G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141546G>T , CM000677.2:g.28141546G>T	GRCh38
NC_000015.9:g.28386692G>T , CM000677.1:g.28386692G>T	GRCh37
NC_000015.8:g.26060287G>T	NCBI36
NG_016355.1:g.185604C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11901C>A MANE Select	ENSP00000261609.8:p.Gly3967=
ENST00000650509.1:c.3612C>A	ENSP00000496936.1:p.Gly1204=
ENST00000261609.11:c.11901C>A	ENSP00000261609.7:p.Gly3967=
NM_004667.5:c.11901C>A	NP_004658.3:p.Gly3967=
XM_005268276.3:c.11787C>A	XP_005268333.1:p.Gly3929=
XM_005268277.3:c.11787C>A	XP_005268334.1:p.Gly3929=
XM_006720726.2:c.11886C>A	XP_006720789.1:p.Gly3962=
XM_006720727.2:c.11643C>A	XP_006720790.1:p.Gly3881=
XM_011522131.1:c.11418C>A	XP_011520433.1:p.Gly3806=
XM_011522132.1:c.9417C>A	XP_011520434.1:p.Gly3139=
XM_011522133.1:c.8646C>A	XP_011520435.1:p.Gly2882=
XM_011522134.1:c.6018C>A	XP_011520436.1:p.Gly2006=
XM_005268276.5:c.11787C>A	XP_005268333.1:p.Gly3929=
XM_006720726.3:c.11886C>A	XP_006720789.1:p.Gly3962=
XM_006720727.3:c.11643C>A	XP_006720790.1:p.Gly3881=
XM_017022695.1:c.11787C>A	XP_016878184.1:p.Gly3929=
XM_017022696.1:c.11787C>A	XP_016878185.1:p.Gly3929=
XM_017022697.1:c.5067C>A	XP_016878186.1:p.Gly1689=
XM_017022698.1:c.5067C>A	XP_016878187.1:p.Gly1689=
NM_004667.6:c.11901C>A MANE Select	NP_004658.3:p.Gly3967=