Canonical Allele Identifier: CA2166480074

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141736C= , CM000677.2:g.28141736C=	GRCh38
NC_000015.9:g.28386882C= , CM000677.1:g.28386882C=	GRCh37
NC_000015.8:g.26060477C=	NCBI36
NG_016355.1:g.185414G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11811G= MANE Select	ENSP00000261609.8:p.Met3937=
ENST00000650509.1:c.3522G=	ENSP00000496936.1:p.Met1174=
ENST00000261609.11:c.11811G=	ENSP00000261609.7:p.Met3937=
NM_004667.5:c.11811G=	NP_004658.3:p.Met3937=
XM_005268276.3:c.11697G=	XP_005268333.1:p.Met3899=
XM_005268277.3:c.11697G=	XP_005268334.1:p.Met3899=
XM_006720726.2:c.11796G=	XP_006720789.1:p.Met3932=
XM_006720727.2:c.11553G=	XP_006720790.1:p.Met3851=
XM_011522131.1:c.11328G=	XP_011520433.1:p.Met3776=
XM_011522132.1:c.9327G=	XP_011520434.1:p.Met3109=
XM_011522133.1:c.8556G=	XP_011520435.1:p.Met2852=
XM_011522134.1:c.5928G=	XP_011520436.1:p.Met1976=
XM_005268276.5:c.11697G=	XP_005268333.1:p.Met3899=
XM_006720726.3:c.11796G=	XP_006720789.1:p.Met3932=
XM_006720727.3:c.11553G=	XP_006720790.1:p.Met3851=
XM_017022695.1:c.11697G=	XP_016878184.1:p.Met3899=
XM_017022696.1:c.11697G=	XP_016878185.1:p.Met3899=
XM_017022697.1:c.4977G=	XP_016878186.1:p.Met1659=
XM_017022698.1:c.4977G=	XP_016878187.1:p.Met1659=
NM_004667.6:c.11811G= MANE Select	NP_004658.3:p.Met3937=