Canonical Allele Identifier: CA489234725

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141513-G-C
• MyVariant Identifiers: chr15:g.28386659G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141513G>C , CM000677.2:g.28141513G>C	GRCh38
NC_000015.9:g.28386659G>C , CM000677.1:g.28386659G>C	GRCh37
NC_000015.8:g.26060254G>C	NCBI36
NG_016355.1:g.185637C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11934C>G MANE Select	ENSP00000261609.8:p.Pro3978=
ENST00000650509.1:c.3645C>G	ENSP00000496936.1:p.Pro1215=
ENST00000261609.11:c.11934C>G	ENSP00000261609.7:p.Pro3978=
NM_004667.5:c.11934C>G	NP_004658.3:p.Pro3978=
XM_005268276.3:c.11820C>G	XP_005268333.1:p.Pro3940=
XM_005268277.3:c.11820C>G	XP_005268334.1:p.Pro3940=
XM_006720726.2:c.11919C>G	XP_006720789.1:p.Pro3973=
XM_006720727.2:c.11676C>G	XP_006720790.1:p.Pro3892=
XM_011522131.1:c.11451C>G	XP_011520433.1:p.Pro3817=
XM_011522132.1:c.9450C>G	XP_011520434.1:p.Pro3150=
XM_011522133.1:c.8679C>G	XP_011520435.1:p.Pro2893=
XM_011522134.1:c.6051C>G	XP_011520436.1:p.Pro2017=
XM_005268276.5:c.11820C>G	XP_005268333.1:p.Pro3940=
XM_006720726.3:c.11919C>G	XP_006720789.1:p.Pro3973=
XM_006720727.3:c.11676C>G	XP_006720790.1:p.Pro3892=
XM_017022695.1:c.11820C>G	XP_016878184.1:p.Pro3940=
XM_017022696.1:c.11820C>G	XP_016878185.1:p.Pro3940=
XM_017022697.1:c.5100C>G	XP_016878186.1:p.Pro1700=
XM_017022698.1:c.5100C>G	XP_016878187.1:p.Pro1700=
NM_004667.6:c.11934C>G MANE Select	NP_004658.3:p.Pro3978=