Canonical Allele Identifier: CA489234672

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386617T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141471T>G , CM000677.2:g.28141471T>G	GRCh38
NC_000015.9:g.28386617T>G , CM000677.1:g.28386617T>G	GRCh37
NC_000015.8:g.26060212T>G	NCBI36
NG_016355.1:g.185679A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11976A>C MANE Select	ENSP00000261609.8:p.Gly3992=
ENST00000650509.1:c.3687A>C	ENSP00000496936.1:p.Gly1229=
ENST00000261609.11:c.11976A>C	ENSP00000261609.7:p.Gly3992=
NM_004667.5:c.11976A>C	NP_004658.3:p.Gly3992=
XM_005268276.3:c.11862A>C	XP_005268333.1:p.Gly3954=
XM_005268277.3:c.11862A>C	XP_005268334.1:p.Gly3954=
XM_006720726.2:c.11961A>C	XP_006720789.1:p.Gly3987=
XM_006720727.2:c.11718A>C	XP_006720790.1:p.Gly3906=
XM_011522131.1:c.11493A>C	XP_011520433.1:p.Gly3831=
XM_011522132.1:c.9492A>C	XP_011520434.1:p.Gly3164=
XM_011522133.1:c.8721A>C	XP_011520435.1:p.Gly2907=
XM_011522134.1:c.6093A>C	XP_011520436.1:p.Gly2031=
XM_005268276.5:c.11862A>C	XP_005268333.1:p.Gly3954=
XM_006720726.3:c.11961A>C	XP_006720789.1:p.Gly3987=
XM_006720727.3:c.11718A>C	XP_006720790.1:p.Gly3906=
XM_017022695.1:c.11862A>C	XP_016878184.1:p.Gly3954=
XM_017022696.1:c.11862A>C	XP_016878185.1:p.Gly3954=
XM_017022697.1:c.5142A>C	XP_016878186.1:p.Gly1714=
XM_017022698.1:c.5142A>C	XP_016878187.1:p.Gly1714=
NM_004667.6:c.11976A>C MANE Select	NP_004658.3:p.Gly3992=