Canonical Allele Identifier: CA1474779926

Gene: HERC5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88499756T= , CM000666.2:g.88499756T=	GRCh38
NC_000004.11:g.89420907T= , CM000666.1:g.89420907T=	GRCh37
NC_000004.10:g.89639930T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264350.8:c.2445-170T= MANE Select	ENSP00000264350.3:n.2445-170T=
ENST00000264350.7:c.2445-170T=	ENSP00000264350.3:n.2445-170T=
ENST00000502913.1:n.1166-170T=
ENST00000508159.1:c.1359-170T=	ENSP00000424129.1:n.1359-170T=
ENST00000510223.5:n.1933-170T=
NM_016323.3:c.2445-170T=	NP_057407.2:n.2445-170T=
XM_011532022.1:c.2220-170T=	XP_011530324.1:n.2220-170T=
XM_011532023.1:c.2157-170T=	XP_011530325.1:n.2157-170T=
XM_011532022.2:c.2673-170T=	XP_011530324.2:n.2673-170T=
NM_016323.4:c.2445-170T= MANE Select	NP_057407.2:n.2445-170T=