Canonical Allele Identifier: CA2166479869

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141505G= , CM000677.2:g.28141505G=	GRCh38
NC_000015.9:g.28386651G= , CM000677.1:g.28386651G=	GRCh37
NC_000015.8:g.26060246G=	NCBI36
NG_016355.1:g.185645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11942C= MANE Select	ENSP00000261609.8:p.Ala3981=
ENST00000650509.1:c.3653C=	ENSP00000496936.1:p.Ala1218=
ENST00000261609.11:c.11942C=	ENSP00000261609.7:p.Ala3981=
NM_004667.5:c.11942C=	NP_004658.3:p.Ala3981=
XM_005268276.3:c.11828C=	XP_005268333.1:p.Ala3943=
XM_005268277.3:c.11828C=	XP_005268334.1:p.Ala3943=
XM_006720726.2:c.11927C=	XP_006720789.1:p.Ala3976=
XM_006720727.2:c.11684C=	XP_006720790.1:p.Ala3895=
XM_011522131.1:c.11459C=	XP_011520433.1:p.Ala3820=
XM_011522132.1:c.9458C=	XP_011520434.1:p.Ala3153=
XM_011522133.1:c.8687C=	XP_011520435.1:p.Ala2896=
XM_011522134.1:c.6059C=	XP_011520436.1:p.Ala2020=
XM_005268276.5:c.11828C=	XP_005268333.1:p.Ala3943=
XM_006720726.3:c.11927C=	XP_006720789.1:p.Ala3976=
XM_006720727.3:c.11684C=	XP_006720790.1:p.Ala3895=
XM_017022695.1:c.11828C=	XP_016878184.1:p.Ala3943=
XM_017022696.1:c.11828C=	XP_016878185.1:p.Ala3943=
XM_017022697.1:c.5108C=	XP_016878186.1:p.Ala1703=
XM_017022698.1:c.5108C=	XP_016878187.1:p.Ala1703=
NM_004667.6:c.11942C= MANE Select	NP_004658.3:p.Ala3981=