Canonical Allele Identifier: CA2166480096

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141785C= , CM000677.2:g.28141785C=	GRCh38
NC_000015.9:g.28386931C= , CM000677.1:g.28386931C=	GRCh37
NC_000015.8:g.26060526C=	NCBI36
NG_016355.1:g.185365G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11762G= MANE Select	ENSP00000261609.8:p.Ser3921=
ENST00000650509.1:c.3473G=	ENSP00000496936.1:p.Ser1158=
ENST00000261609.11:c.11762G=	ENSP00000261609.7:p.Ser3921=
ENST00000564519.1:n.277G=
NM_004667.5:c.11762G=	NP_004658.3:p.Ser3921=
XM_005268276.3:c.11648G=	XP_005268333.1:p.Ser3883=
XM_005268277.3:c.11648G=	XP_005268334.1:p.Ser3883=
XM_006720726.2:c.11747G=	XP_006720789.1:p.Ser3916=
XM_006720727.2:c.11504G=	XP_006720790.1:p.Ser3835=
XM_011522131.1:c.11279G=	XP_011520433.1:p.Ser3760=
XM_011522132.1:c.9278G=	XP_011520434.1:p.Ser3093=
XM_011522133.1:c.8507G=	XP_011520435.1:p.Ser2836=
XM_011522134.1:c.5879G=	XP_011520436.1:p.Ser1960=
XM_005268276.5:c.11648G=	XP_005268333.1:p.Ser3883=
XM_006720726.3:c.11747G=	XP_006720789.1:p.Ser3916=
XM_006720727.3:c.11504G=	XP_006720790.1:p.Ser3835=
XM_017022695.1:c.11648G=	XP_016878184.1:p.Ser3883=
XM_017022696.1:c.11648G=	XP_016878185.1:p.Ser3883=
XM_017022697.1:c.4928G=	XP_016878186.1:p.Ser1643=
XM_017022698.1:c.4928G=	XP_016878187.1:p.Ser1643=
NM_004667.6:c.11762G= MANE Select	NP_004658.3:p.Ser3921=