Canonical Allele Identifier: CA799652409

Gene: HERC5

Linked Data

• dbSNP Id: rs1319750909
• MyVariant Identifiers: chr4:g.89420923C>G (hg19) ; chr4:g.88499772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88499772C>G , CM000666.2:g.88499772C>G	GRCh38
NC_000004.11:g.89420923C>G , CM000666.1:g.89420923C>G	GRCh37
NC_000004.10:g.89639946C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264350.8:c.2445-154C>G MANE Select	ENSP00000264350.3:n.2445-154C>G
ENST00000264350.7:c.2445-154C>G	ENSP00000264350.3:n.2445-154C>G
ENST00000502913.1:n.1166-154C>G
ENST00000508159.1:c.1359-154C>G	ENSP00000424129.1:n.1359-154C>G
ENST00000510223.5:n.1933-154C>G
NM_016323.3:c.2445-154C>G	NP_057407.2:n.2445-154C>G
XM_011532022.1:c.2220-154C>G	XP_011530324.1:n.2220-154C>G
XM_011532023.1:c.2157-154C>G	XP_011530325.1:n.2157-154C>G
XM_011532022.2:c.2673-154C>G	XP_011530324.2:n.2673-154C>G
NM_016323.4:c.2445-154C>G MANE Select	NP_057407.2:n.2445-154C>G