Canonical Allele Identifier: CA1474779975

Gene: HERC5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88499893_88499898delinsACCTTT , CM000666.2:g.88499893_88499898delinsACCTTT	GRCh38
NC_000004.11:g.89421044_89421049delinsACCTTT , CM000666.1:g.89421044_89421049delinsACCTTT	GRCh37
NC_000004.10:g.89640067_89640072delinsACCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264350.8:c.2445-33_2445-28delinsACCTTT MANE Select	ENSP00000264350.3:n.2445-33_2445-28delinsACCTTT
ENST00000264350.7:c.2445-33_2445-28delinsACCTTT	ENSP00000264350.3:n.2445-33_2445-28delinsACCTTT
ENST00000502913.1:n.1166-33_1166-28delinsACCTTT
ENST00000508159.1:c.1359-33_1359-28delinsACCTTT	ENSP00000424129.1:n.1359-33_1359-28delinsACCTTT
ENST00000510223.5:n.1933-33_1933-28delinsACCTTT
NM_016323.3:c.2445-33_2445-28delinsACCTTT	NP_057407.2:n.2445-33_2445-28delinsACCTTT
XM_011532022.1:c.2220-33_2220-28delinsACCTTT	XP_011530324.1:n.2220-33_2220-28delinsACCTTT
XM_011532023.1:c.2157-33_2157-28delinsACCTTT	XP_011530325.1:n.2157-33_2157-28delinsACCTTT
XM_011532022.2:c.2673-33_2673-28delinsACCTTT	XP_011530324.2:n.2673-33_2673-28delinsACCTTT
NM_016323.4:c.2445-33_2445-28delinsACCTTT MANE Select	NP_057407.2:n.2445-33_2445-28delinsACCTTT