Canonical Allele Identifier: CA2166480033

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141689A= , CM000677.2:g.28141689A=	GRCh38
NC_000015.9:g.28386835A= , CM000677.1:g.28386835A=	GRCh37
NC_000015.8:g.26060430A=	NCBI36
NG_016355.1:g.185461T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11816+42T= MANE Select	ENSP00000261609.8:n.11816+42T=
ENST00000650509.1:c.3527+42T=	ENSP00000496936.1:n.3527+42T=
ENST00000261609.11:c.11816+42T=	ENSP00000261609.7:n.11816+42T=
NM_004667.5:c.11816+42T=	NP_004658.3:n.11816+42T=
XM_005268276.3:c.11702+42T=	XP_005268333.1:n.11702+42T=
XM_005268277.3:c.11702+42T=	XP_005268334.1:n.11702+42T=
XM_006720726.2:c.11801+42T=	XP_006720789.1:n.11801+42T=
XM_006720727.2:c.11558+42T=	XP_006720790.1:n.11558+42T=
XM_011522131.1:c.11333+42T=	XP_011520433.1:n.11333+42T=
XM_011522132.1:c.9332+42T=	XP_011520434.1:n.9332+42T=
XM_011522133.1:c.8561+42T=	XP_011520435.1:n.8561+42T=
XM_011522134.1:c.5933+42T=	XP_011520436.1:n.5933+42T=
XM_005268276.5:c.11702+42T=	XP_005268333.1:n.11702+42T=
XM_006720726.3:c.11801+42T=	XP_006720789.1:n.11801+42T=
XM_006720727.3:c.11558+42T=	XP_006720790.1:n.11558+42T=
XM_017022695.1:c.11702+42T=	XP_016878184.1:n.11702+42T=
XM_017022696.1:c.11702+42T=	XP_016878185.1:n.11702+42T=
XM_017022697.1:c.4982+42T=	XP_016878186.1:n.4982+42T=
XM_017022698.1:c.4982+42T=	XP_016878187.1:n.4982+42T=
NM_004667.6:c.11816+42T= MANE Select	NP_004658.3:n.11816+42T=