Canonical Allele Identifier: CA1917104705

Gene: HERC4

Linked Data

• dbSNP Id: rs566397547

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67923600C>A , CM000672.2:g.67923600C>A	GRCh38
NC_000010.10:g.69683357C>A , CM000672.1:g.69683357C>A	GRCh37
NC_000010.9:g.69353363C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373700.9:c.2942-461G>T MANE Select	ENSP00000362804.4:n.2942-461G>T
ENST00000277817.10:c.2636-461G>T	ENSP00000277817.6:n.2636-461G>T
ENST00000373700.8:c.2942-461G>T	ENSP00000362804.4:n.2942-461G>T
ENST00000395198.7:c.2966-461G>T	ENSP00000378624.3:n.2966-461G>T
ENST00000412272.6:c.2732-461G>T	ENSP00000416504.2:n.2732-461G>T
ENST00000427635.6:c.5736-461G>T
ENST00000473533.6:c.*2336-461G>T	ENSP00000423671.1:n.*2336-461G>T
NM_001278185.1:c.2732-461G>T	NP_001265114.1:n.2732-461G>T
NM_001278186.1:c.2177-461G>T	NP_001265115.1:n.2177-461G>T
NM_015601.3:c.2942-461G>T	NP_056416.2:n.2942-461G>T
NM_022079.2:c.2966-461G>T	NP_071362.1:n.2966-461G>T
XM_011539592.1:c.3038-461G>T	XP_011537894.1:n.3038-461G>T
XM_011539593.1:c.3014-461G>T	XP_011537895.1:n.3014-461G>T
XM_011539594.1:c.2828-461G>T	XP_011537896.1:n.2828-461G>T
XM_011539595.1:c.2828-461G>T	XP_011537897.1:n.2828-461G>T
XM_011539596.1:c.2756-461G>T	XP_011537898.1:n.2756-461G>T
XM_011539597.1:c.2675-461G>T	XP_011537899.1:n.2675-461G>T
XM_011539592.3:c.3038-461G>T	XP_011537894.1:n.3038-461G>T
XM_011539593.3:c.3014-461G>T	XP_011537895.1:n.3014-461G>T
XM_011539594.2:c.2828-461G>T	XP_011537896.1:n.2828-461G>T
XM_011539595.2:c.2828-461G>T	XP_011537897.1:n.2828-461G>T
XM_011539596.2:c.2756-461G>T	XP_011537898.1:n.2756-461G>T
XM_011539597.3:c.2675-461G>T	XP_011537899.1:n.2675-461G>T
XM_017016041.2:c.2603-461G>T	XP_016871530.1:n.2603-461G>T
XM_024447927.1:c.3038-461G>T	XP_024303695.1:n.3038-461G>T
XM_024447928.1:c.3038-461G>T	XP_024303696.1:n.3038-461G>T
XM_024447929.1:c.2966-461G>T	XP_024303697.1:n.2966-461G>T
XM_024447930.1:c.2966-461G>T	XP_024303698.1:n.2966-461G>T
XM_024447931.1:c.2942-461G>T	XP_024303699.1:n.2942-461G>T
XM_024447932.1:c.1421-461G>T	XP_024303700.1:n.1421-461G>T
NM_001278185.2:c.2732-461G>T	NP_001265114.1:n.2732-461G>T
NM_001278186.2:c.2177-461G>T	NP_001265115.1:n.2177-461G>T
NM_015601.4:c.2942-461G>T MANE Select	NP_056416.2:n.2942-461G>T
NM_022079.3:c.2966-461G>T	NP_071362.1:n.2966-461G>T