Canonical Allele Identifier: CA489234868

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386731A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141585A>G , CM000677.2:g.28141585A>G	GRCh38
NC_000015.9:g.28386731A>G , CM000677.1:g.28386731A>G	GRCh37
NC_000015.8:g.26060326A>G	NCBI36
NG_016355.1:g.185565T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11862T>C MANE Select	ENSP00000261609.8:p.Ile3954=
ENST00000650509.1:c.3573T>C	ENSP00000496936.1:p.Ile1191=
ENST00000261609.11:c.11862T>C	ENSP00000261609.7:p.Ile3954=
NM_004667.5:c.11862T>C	NP_004658.3:p.Ile3954=
XM_005268276.3:c.11748T>C	XP_005268333.1:p.Ile3916=
XM_005268277.3:c.11748T>C	XP_005268334.1:p.Ile3916=
XM_006720726.2:c.11847T>C	XP_006720789.1:p.Ile3949=
XM_006720727.2:c.11604T>C	XP_006720790.1:p.Ile3868=
XM_011522131.1:c.11379T>C	XP_011520433.1:p.Ile3793=
XM_011522132.1:c.9378T>C	XP_011520434.1:p.Ile3126=
XM_011522133.1:c.8607T>C	XP_011520435.1:p.Ile2869=
XM_011522134.1:c.5979T>C	XP_011520436.1:p.Ile1993=
XM_005268276.5:c.11748T>C	XP_005268333.1:p.Ile3916=
XM_006720726.3:c.11847T>C	XP_006720789.1:p.Ile3949=
XM_006720727.3:c.11604T>C	XP_006720790.1:p.Ile3868=
XM_017022695.1:c.11748T>C	XP_016878184.1:p.Ile3916=
XM_017022696.1:c.11748T>C	XP_016878185.1:p.Ile3916=
XM_017022697.1:c.5028T>C	XP_016878186.1:p.Ile1676=
XM_017022698.1:c.5028T>C	XP_016878187.1:p.Ile1676=
NM_004667.6:c.11862T>C MANE Select	NP_004658.3:p.Ile3954=