Canonical Allele Identifier: CA489234775

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386704G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141558G>C , CM000677.2:g.28141558G>C	GRCh38
NC_000015.9:g.28386704G>C , CM000677.1:g.28386704G>C	GRCh37
NC_000015.8:g.26060299G>C	NCBI36
NG_016355.1:g.185592C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11889C>G MANE Select	ENSP00000261609.8:p.Gly3963=
ENST00000650509.1:c.3600C>G	ENSP00000496936.1:p.Gly1200=
ENST00000261609.11:c.11889C>G	ENSP00000261609.7:p.Gly3963=
NM_004667.5:c.11889C>G	NP_004658.3:p.Gly3963=
XM_005268276.3:c.11775C>G	XP_005268333.1:p.Gly3925=
XM_005268277.3:c.11775C>G	XP_005268334.1:p.Gly3925=
XM_006720726.2:c.11874C>G	XP_006720789.1:p.Gly3958=
XM_006720727.2:c.11631C>G	XP_006720790.1:p.Gly3877=
XM_011522131.1:c.11406C>G	XP_011520433.1:p.Gly3802=
XM_011522132.1:c.9405C>G	XP_011520434.1:p.Gly3135=
XM_011522133.1:c.8634C>G	XP_011520435.1:p.Gly2878=
XM_011522134.1:c.6006C>G	XP_011520436.1:p.Gly2002=
XM_005268276.5:c.11775C>G	XP_005268333.1:p.Gly3925=
XM_006720726.3:c.11874C>G	XP_006720789.1:p.Gly3958=
XM_006720727.3:c.11631C>G	XP_006720790.1:p.Gly3877=
XM_017022695.1:c.11775C>G	XP_016878184.1:p.Gly3925=
XM_017022696.1:c.11775C>G	XP_016878185.1:p.Gly3925=
XM_017022697.1:c.5055C>G	XP_016878186.1:p.Gly1685=
XM_017022698.1:c.5055C>G	XP_016878187.1:p.Gly1685=
NM_004667.6:c.11889C>G MANE Select	NP_004658.3:p.Gly3963=