Canonical Allele Identifier: CA2166480104

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141801C= , CM000677.2:g.28141801C=	GRCh38
NC_000015.9:g.28386947C= , CM000677.1:g.28386947C=	GRCh37
NC_000015.8:g.26060542C=	NCBI36
NG_016355.1:g.185349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11746G= MANE Select	ENSP00000261609.8:p.Asp3916=
ENST00000650509.1:c.3457G=	ENSP00000496936.1:p.Asp1153=
ENST00000261609.11:c.11746G=	ENSP00000261609.7:p.Asp3916=
ENST00000564519.1:n.261G=
NM_004667.5:c.11746G=	NP_004658.3:p.Asp3916=
XM_005268276.3:c.11632G=	XP_005268333.1:p.Asp3878=
XM_005268277.3:c.11632G=	XP_005268334.1:p.Asp3878=
XM_006720726.2:c.11731G=	XP_006720789.1:p.Asp3911=
XM_006720727.2:c.11488G=	XP_006720790.1:p.Asp3830=
XM_011522131.1:c.11263G=	XP_011520433.1:p.Asp3755=
XM_011522132.1:c.9262G=	XP_011520434.1:p.Asp3088=
XM_011522133.1:c.8491G=	XP_011520435.1:p.Asp2831=
XM_011522134.1:c.5863G=	XP_011520436.1:p.Asp1955=
XM_005268276.5:c.11632G=	XP_005268333.1:p.Asp3878=
XM_006720726.3:c.11731G=	XP_006720789.1:p.Asp3911=
XM_006720727.3:c.11488G=	XP_006720790.1:p.Asp3830=
XM_017022695.1:c.11632G=	XP_016878184.1:p.Asp3878=
XM_017022696.1:c.11632G=	XP_016878185.1:p.Asp3878=
XM_017022697.1:c.4912G=	XP_016878186.1:p.Asp1638=
XM_017022698.1:c.4912G=	XP_016878187.1:p.Asp1638=
NM_004667.6:c.11746G= MANE Select	NP_004658.3:p.Asp3916=