Canonical Allele Identifier: CA2166480092

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141775A= , CM000677.2:g.28141775A=	GRCh38
NC_000015.9:g.28386921A= , CM000677.1:g.28386921A=	GRCh37
NC_000015.8:g.26060516A=	NCBI36
NG_016355.1:g.185375T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11772T= MANE Select	ENSP00000261609.8:p.Ile3924=
ENST00000650509.1:c.3483T=	ENSP00000496936.1:p.Ile1161=
ENST00000261609.11:c.11772T=	ENSP00000261609.7:p.Ile3924=
ENST00000564519.1:n.287T=
NM_004667.5:c.11772T=	NP_004658.3:p.Ile3924=
XM_005268276.3:c.11658T=	XP_005268333.1:p.Ile3886=
XM_005268277.3:c.11658T=	XP_005268334.1:p.Ile3886=
XM_006720726.2:c.11757T=	XP_006720789.1:p.Ile3919=
XM_006720727.2:c.11514T=	XP_006720790.1:p.Ile3838=
XM_011522131.1:c.11289T=	XP_011520433.1:p.Ile3763=
XM_011522132.1:c.9288T=	XP_011520434.1:p.Ile3096=
XM_011522133.1:c.8517T=	XP_011520435.1:p.Ile2839=
XM_011522134.1:c.5889T=	XP_011520436.1:p.Ile1963=
XM_005268276.5:c.11658T=	XP_005268333.1:p.Ile3886=
XM_006720726.3:c.11757T=	XP_006720789.1:p.Ile3919=
XM_006720727.3:c.11514T=	XP_006720790.1:p.Ile3838=
XM_017022695.1:c.11658T=	XP_016878184.1:p.Ile3886=
XM_017022696.1:c.11658T=	XP_016878185.1:p.Ile3886=
XM_017022697.1:c.4938T=	XP_016878186.1:p.Ile1646=
XM_017022698.1:c.4938T=	XP_016878187.1:p.Ile1646=
NM_004667.6:c.11772T= MANE Select	NP_004658.3:p.Ile3924=