Canonical Allele Identifier: CA2166480087

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141757G= , CM000677.2:g.28141757G=	GRCh38
NC_000015.9:g.28386903G= , CM000677.1:g.28386903G=	GRCh37
NC_000015.8:g.26060498G=	NCBI36
NG_016355.1:g.185393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11790C= MANE Select	ENSP00000261609.8:p.Asp3930=
ENST00000650509.1:c.3501C=	ENSP00000496936.1:p.Asp1167=
ENST00000261609.11:c.11790C=	ENSP00000261609.7:p.Asp3930=
ENST00000564519.1:n.305C=
NM_004667.5:c.11790C=	NP_004658.3:p.Asp3930=
XM_005268276.3:c.11676C=	XP_005268333.1:p.Asp3892=
XM_005268277.3:c.11676C=	XP_005268334.1:p.Asp3892=
XM_006720726.2:c.11775C=	XP_006720789.1:p.Asp3925=
XM_006720727.2:c.11532C=	XP_006720790.1:p.Asp3844=
XM_011522131.1:c.11307C=	XP_011520433.1:p.Asp3769=
XM_011522132.1:c.9306C=	XP_011520434.1:p.Asp3102=
XM_011522133.1:c.8535C=	XP_011520435.1:p.Asp2845=
XM_011522134.1:c.5907C=	XP_011520436.1:p.Asp1969=
XM_005268276.5:c.11676C=	XP_005268333.1:p.Asp3892=
XM_006720726.3:c.11775C=	XP_006720789.1:p.Asp3925=
XM_006720727.3:c.11532C=	XP_006720790.1:p.Asp3844=
XM_017022695.1:c.11676C=	XP_016878184.1:p.Asp3892=
XM_017022696.1:c.11676C=	XP_016878185.1:p.Asp3892=
XM_017022697.1:c.4956C=	XP_016878186.1:p.Asp1652=
XM_017022698.1:c.4956C=	XP_016878187.1:p.Asp1652=
NM_004667.6:c.11790C= MANE Select	NP_004658.3:p.Asp3930=