Canonical Allele Identifier: CA2166480111

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141818G= , CM000677.2:g.28141818G=	GRCh38
NC_000015.9:g.28386964G= , CM000677.1:g.28386964G=	GRCh37
NC_000015.8:g.26060559G=	NCBI36
NG_016355.1:g.185332C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11729C= MANE Select	ENSP00000261609.8:p.Ala3910=
ENST00000650509.1:c.3440C=	ENSP00000496936.1:p.Ala1147=
ENST00000261609.11:c.11729C=	ENSP00000261609.7:p.Ala3910=
ENST00000564519.1:n.244C=
NM_004667.5:c.11729C=	NP_004658.3:p.Ala3910=
XM_005268276.3:c.11615C=	XP_005268333.1:p.Ala3872=
XM_005268277.3:c.11615C=	XP_005268334.1:p.Ala3872=
XM_006720726.2:c.11714C=	XP_006720789.1:p.Ala3905=
XM_006720727.2:c.11471C=	XP_006720790.1:p.Ala3824=
XM_011522131.1:c.11246C=	XP_011520433.1:p.Ala3749=
XM_011522132.1:c.9245C=	XP_011520434.1:p.Ala3082=
XM_011522133.1:c.8474C=	XP_011520435.1:p.Ala2825=
XM_011522134.1:c.5846C=	XP_011520436.1:p.Ala1949=
XM_005268276.5:c.11615C=	XP_005268333.1:p.Ala3872=
XM_006720726.3:c.11714C=	XP_006720789.1:p.Ala3905=
XM_006720727.3:c.11471C=	XP_006720790.1:p.Ala3824=
XM_017022695.1:c.11615C=	XP_016878184.1:p.Ala3872=
XM_017022696.1:c.11615C=	XP_016878185.1:p.Ala3872=
XM_017022697.1:c.4895C=	XP_016878186.1:p.Ala1632=
XM_017022698.1:c.4895C=	XP_016878187.1:p.Ala1632=
NM_004667.6:c.11729C= MANE Select	NP_004658.3:p.Ala3910=