Canonical Allele Identifier: CA2166479845

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141480C= , CM000677.2:g.28141480C=	GRCh38
NC_000015.9:g.28386626C= , CM000677.1:g.28386626C=	GRCh37
NC_000015.8:g.26060221C=	NCBI36
NG_016355.1:g.185670G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.11967G= MANE Select	ENSP00000261609.8:p.Gln3989=
ENST00000650509.1:c.3678G=	ENSP00000496936.1:p.Gln1226=
ENST00000261609.11:c.11967G=	ENSP00000261609.7:p.Gln3989=
NM_004667.5:c.11967G=	NP_004658.3:p.Gln3989=
XM_005268276.3:c.11853G=	XP_005268333.1:p.Gln3951=
XM_005268277.3:c.11853G=	XP_005268334.1:p.Gln3951=
XM_006720726.2:c.11952G=	XP_006720789.1:p.Gln3984=
XM_006720727.2:c.11709G=	XP_006720790.1:p.Gln3903=
XM_011522131.1:c.11484G=	XP_011520433.1:p.Gln3828=
XM_011522132.1:c.9483G=	XP_011520434.1:p.Gln3161=
XM_011522133.1:c.8712G=	XP_011520435.1:p.Gln2904=
XM_011522134.1:c.6084G=	XP_011520436.1:p.Gln2028=
XM_005268276.5:c.11853G=	XP_005268333.1:p.Gln3951=
XM_006720726.3:c.11952G=	XP_006720789.1:p.Gln3984=
XM_006720727.3:c.11709G=	XP_006720790.1:p.Gln3903=
XM_017022695.1:c.11853G=	XP_016878184.1:p.Gln3951=
XM_017022696.1:c.11853G=	XP_016878185.1:p.Gln3951=
XM_017022697.1:c.5133G=	XP_016878186.1:p.Gln1711=
XM_017022698.1:c.5133G=	XP_016878187.1:p.Gln1711=
NM_004667.6:c.11967G= MANE Select	NP_004658.3:p.Gln3989=