Canonical Allele Identifier: CA2166480114

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141822T= , CM000677.2:g.28141822T=	GRCh38
NC_000015.9:g.28386968T= , CM000677.1:g.28386968T=	GRCh37
NC_000015.8:g.26060563T=	NCBI36
NG_016355.1:g.185328A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11725A= MANE Select	ENSP00000261609.8:p.Met3909=
ENST00000650509.1:c.3436A=	ENSP00000496936.1:p.Met1146=
ENST00000261609.11:c.11725A=	ENSP00000261609.7:p.Met3909=
ENST00000564519.1:n.240A=
NM_004667.5:c.11725A=	NP_004658.3:p.Met3909=
XM_005268276.3:c.11611A=	XP_005268333.1:p.Met3871=
XM_005268277.3:c.11611A=	XP_005268334.1:p.Met3871=
XM_006720726.2:c.11710A=	XP_006720789.1:p.Met3904=
XM_006720727.2:c.11467A=	XP_006720790.1:p.Met3823=
XM_011522131.1:c.11242A=	XP_011520433.1:p.Met3748=
XM_011522132.1:c.9241A=	XP_011520434.1:p.Met3081=
XM_011522133.1:c.8470A=	XP_011520435.1:p.Met2824=
XM_011522134.1:c.5842A=	XP_011520436.1:p.Met1948=
XM_005268276.5:c.11611A=	XP_005268333.1:p.Met3871=
XM_006720726.3:c.11710A=	XP_006720789.1:p.Met3904=
XM_006720727.3:c.11467A=	XP_006720790.1:p.Met3823=
XM_017022695.1:c.11611A=	XP_016878184.1:p.Met3871=
XM_017022696.1:c.11611A=	XP_016878185.1:p.Met3871=
XM_017022697.1:c.4891A=	XP_016878186.1:p.Met1631=
XM_017022698.1:c.4891A=	XP_016878187.1:p.Met1631=
NM_004667.6:c.11725A= MANE Select	NP_004658.3:p.Met3909=