Canonical Allele Identifier: CA489235069

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141814-G-A
• MyVariant Identifiers: chr15:g.28386960G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141814G>A , CM000677.2:g.28141814G>A	GRCh38
NC_000015.9:g.28386960G>A , CM000677.1:g.28386960G>A	GRCh37
NC_000015.8:g.26060555G>A	NCBI36
NG_016355.1:g.185336C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11733C>T MANE Select	ENSP00000261609.8:p.Asp3911=
ENST00000650509.1:c.3444C>T	ENSP00000496936.1:p.Asp1148=
ENST00000261609.11:c.11733C>T	ENSP00000261609.7:p.Asp3911=
ENST00000564519.1:n.248C>T
NM_004667.5:c.11733C>T	NP_004658.3:p.Asp3911=
XM_005268276.3:c.11619C>T	XP_005268333.1:p.Asp3873=
XM_005268277.3:c.11619C>T	XP_005268334.1:p.Asp3873=
XM_006720726.2:c.11718C>T	XP_006720789.1:p.Asp3906=
XM_006720727.2:c.11475C>T	XP_006720790.1:p.Asp3825=
XM_011522131.1:c.11250C>T	XP_011520433.1:p.Asp3750=
XM_011522132.1:c.9249C>T	XP_011520434.1:p.Asp3083=
XM_011522133.1:c.8478C>T	XP_011520435.1:p.Asp2826=
XM_011522134.1:c.5850C>T	XP_011520436.1:p.Asp1950=
XM_005268276.5:c.11619C>T	XP_005268333.1:p.Asp3873=
XM_006720726.3:c.11718C>T	XP_006720789.1:p.Asp3906=
XM_006720727.3:c.11475C>T	XP_006720790.1:p.Asp3825=
XM_017022695.1:c.11619C>T	XP_016878184.1:p.Asp3873=
XM_017022696.1:c.11619C>T	XP_016878185.1:p.Asp3873=
XM_017022697.1:c.4899C>T	XP_016878186.1:p.Asp1633=
XM_017022698.1:c.4899C>T	XP_016878187.1:p.Asp1633=
NM_004667.6:c.11733C>T MANE Select	NP_004658.3:p.Asp3911=