Canonical Allele Identifier: CA2166479872

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141510A= , CM000677.2:g.28141510A=	GRCh38
NC_000015.9:g.28386656A= , CM000677.1:g.28386656A=	GRCh37
NC_000015.8:g.26060251A=	NCBI36
NG_016355.1:g.185640T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11937T= MANE Select	ENSP00000261609.8:p.Cys3979=
ENST00000650509.1:c.3648T=	ENSP00000496936.1:p.Cys1216=
ENST00000261609.11:c.11937T=	ENSP00000261609.7:p.Cys3979=
NM_004667.5:c.11937T=	NP_004658.3:p.Cys3979=
XM_005268276.3:c.11823T=	XP_005268333.1:p.Cys3941=
XM_005268277.3:c.11823T=	XP_005268334.1:p.Cys3941=
XM_006720726.2:c.11922T=	XP_006720789.1:p.Cys3974=
XM_006720727.2:c.11679T=	XP_006720790.1:p.Cys3893=
XM_011522131.1:c.11454T=	XP_011520433.1:p.Cys3818=
XM_011522132.1:c.9453T=	XP_011520434.1:p.Cys3151=
XM_011522133.1:c.8682T=	XP_011520435.1:p.Cys2894=
XM_011522134.1:c.6054T=	XP_011520436.1:p.Cys2018=
XM_005268276.5:c.11823T=	XP_005268333.1:p.Cys3941=
XM_006720726.3:c.11922T=	XP_006720789.1:p.Cys3974=
XM_006720727.3:c.11679T=	XP_006720790.1:p.Cys3893=
XM_017022695.1:c.11823T=	XP_016878184.1:p.Cys3941=
XM_017022696.1:c.11823T=	XP_016878185.1:p.Cys3941=
XM_017022697.1:c.5103T=	XP_016878186.1:p.Cys1701=
XM_017022698.1:c.5103T=	XP_016878187.1:p.Cys1701=
NM_004667.6:c.11937T= MANE Select	NP_004658.3:p.Cys3979=