Canonical Allele Identifier: CA267916333

Gene: HERC2

Linked Data

• dbSNP Id: rs35772638
• MyVariant Identifiers: chr15:g.28356681_28356682insG (hg19) ; chr15:g.28111535_28111536insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111538dup , CM000677.2:g.28111538dup	GRCh38
NC_000015.9:g.28356684dup , CM000677.1:g.28356684dup	GRCh37
NC_000015.8:g.26030279dup	NCBI36
NG_016355.1:g.215614dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.*227dup MANE Select	ENSP00000261609.8:n.*227dup
ENST00000650509.1:c.6211dup	ENSP00000496936.1:n.6211dup
ENST00000261609.11:c.*227dup	ENSP00000261609.7:n.*227dup
ENST00000566635.5:n.1857dup
NM_004667.5:c.*227dup	NP_004658.3:n.*227dup
XM_005268276.3:c.*227dup	XP_005268333.1:n.*227dup
XM_005268277.3:c.*227dup	XP_005268334.1:n.*227dup
XM_006720726.2:c.*227dup	XP_006720789.1:n.*227dup
XM_006720727.2:c.*227dup	XP_006720790.1:n.*227dup
XM_011522131.1:c.*227dup	XP_011520433.1:n.*227dup
XM_011522132.1:c.*227dup	XP_011520434.1:n.*227dup
XM_011522133.1:c.*227dup	XP_011520435.1:n.*227dup
XM_011522134.1:c.*227dup	XP_011520436.1:n.*227dup
XM_005268276.5:c.*227dup	XP_005268333.1:n.*227dup
XM_006720726.3:c.*227dup	XP_006720789.1:n.*227dup
XM_006720727.3:c.*227dup	XP_006720790.1:n.*227dup
XM_017022695.1:c.*227dup	XP_016878184.1:n.*227dup
XM_017022696.1:c.*227dup	XP_016878185.1:n.*227dup
XM_017022697.1:c.*227dup	XP_016878186.1:n.*227dup
XM_017022698.1:c.*227dup	XP_016878187.1:n.*227dup
NM_004667.6:c.*227dup MANE Select	NP_004658.3:n.*227dup