Canonical Allele Identifier: CA489234764

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386689A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141543A>T , CM000677.2:g.28141543A>T	GRCh38
NC_000015.9:g.28386689A>T , CM000677.1:g.28386689A>T	GRCh37
NC_000015.8:g.26060284A>T	NCBI36
NG_016355.1:g.185607T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11904T>A MANE Select	ENSP00000261609.8:p.Ile3968=
ENST00000650509.1:c.3615T>A	ENSP00000496936.1:p.Ile1205=
ENST00000261609.11:c.11904T>A	ENSP00000261609.7:p.Ile3968=
NM_004667.5:c.11904T>A	NP_004658.3:p.Ile3968=
XM_005268276.3:c.11790T>A	XP_005268333.1:p.Ile3930=
XM_005268277.3:c.11790T>A	XP_005268334.1:p.Ile3930=
XM_006720726.2:c.11889T>A	XP_006720789.1:p.Ile3963=
XM_006720727.2:c.11646T>A	XP_006720790.1:p.Ile3882=
XM_011522131.1:c.11421T>A	XP_011520433.1:p.Ile3807=
XM_011522132.1:c.9420T>A	XP_011520434.1:p.Ile3140=
XM_011522133.1:c.8649T>A	XP_011520435.1:p.Ile2883=
XM_011522134.1:c.6021T>A	XP_011520436.1:p.Ile2007=
XM_005268276.5:c.11790T>A	XP_005268333.1:p.Ile3930=
XM_006720726.3:c.11889T>A	XP_006720789.1:p.Ile3963=
XM_006720727.3:c.11646T>A	XP_006720790.1:p.Ile3882=
XM_017022695.1:c.11790T>A	XP_016878184.1:p.Ile3930=
XM_017022696.1:c.11790T>A	XP_016878185.1:p.Ile3930=
XM_017022697.1:c.5070T>A	XP_016878186.1:p.Ile1690=
XM_017022698.1:c.5070T>A	XP_016878187.1:p.Ile1690=
NM_004667.6:c.11904T>A MANE Select	NP_004658.3:p.Ile3968=