Canonical Allele Identifier: CA489235027

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386914T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141768T>G , CM000677.2:g.28141768T>G	GRCh38
NC_000015.9:g.28386914T>G , CM000677.1:g.28386914T>G	GRCh37
NC_000015.8:g.26060509T>G	NCBI36
NG_016355.1:g.185382A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11779A>C MANE Select	ENSP00000261609.8:p.Arg3927=
ENST00000650509.1:c.3490A>C	ENSP00000496936.1:p.Arg1164=
ENST00000261609.11:c.11779A>C	ENSP00000261609.7:p.Arg3927=
ENST00000564519.1:n.294A>C
NM_004667.5:c.11779A>C	NP_004658.3:p.Arg3927=
XM_005268276.3:c.11665A>C	XP_005268333.1:p.Arg3889=
XM_005268277.3:c.11665A>C	XP_005268334.1:p.Arg3889=
XM_006720726.2:c.11764A>C	XP_006720789.1:p.Arg3922=
XM_006720727.2:c.11521A>C	XP_006720790.1:p.Arg3841=
XM_011522131.1:c.11296A>C	XP_011520433.1:p.Arg3766=
XM_011522132.1:c.9295A>C	XP_011520434.1:p.Arg3099=
XM_011522133.1:c.8524A>C	XP_011520435.1:p.Arg2842=
XM_011522134.1:c.5896A>C	XP_011520436.1:p.Arg1966=
XM_005268276.5:c.11665A>C	XP_005268333.1:p.Arg3889=
XM_006720726.3:c.11764A>C	XP_006720789.1:p.Arg3922=
XM_006720727.3:c.11521A>C	XP_006720790.1:p.Arg3841=
XM_017022695.1:c.11665A>C	XP_016878184.1:p.Arg3889=
XM_017022696.1:c.11665A>C	XP_016878185.1:p.Arg3889=
XM_017022697.1:c.4945A>C	XP_016878186.1:p.Arg1649=
XM_017022698.1:c.4945A>C	XP_016878187.1:p.Arg1649=
NM_004667.6:c.11779A>C MANE Select	NP_004658.3:p.Arg3927=