Canonical Allele Identifier: CA667770004

Gene: HERC4

Linked Data

• dbSNP Id: rs1356504232
• gnomAD v3: 10-67923615-A-C
• gnomAD v4: 10-67923615-A-C
• MyVariant Identifiers: chr10:g.69683372A>C (hg19) ; chr10:g.67923615A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67923615A>C , CM000672.2:g.67923615A>C	GRCh38
NC_000010.10:g.69683372A>C , CM000672.1:g.69683372A>C	GRCh37
NC_000010.9:g.69353378A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373700.9:c.2942-476T>G MANE Select	ENSP00000362804.4:n.2942-476T>G
ENST00000277817.10:c.2636-476T>G	ENSP00000277817.6:n.2636-476T>G
ENST00000373700.8:c.2942-476T>G	ENSP00000362804.4:n.2942-476T>G
ENST00000395198.7:c.2966-476T>G	ENSP00000378624.3:n.2966-476T>G
ENST00000412272.6:c.2732-476T>G	ENSP00000416504.2:n.2732-476T>G
ENST00000427635.6:c.5736-476T>G
ENST00000473533.6:c.*2336-476T>G	ENSP00000423671.1:n.*2336-476T>G
NM_001278185.1:c.2732-476T>G	NP_001265114.1:n.2732-476T>G
NM_001278186.1:c.2177-476T>G	NP_001265115.1:n.2177-476T>G
NM_015601.3:c.2942-476T>G	NP_056416.2:n.2942-476T>G
NM_022079.2:c.2966-476T>G	NP_071362.1:n.2966-476T>G
XM_011539592.1:c.3038-476T>G	XP_011537894.1:n.3038-476T>G
XM_011539593.1:c.3014-476T>G	XP_011537895.1:n.3014-476T>G
XM_011539594.1:c.2828-476T>G	XP_011537896.1:n.2828-476T>G
XM_011539595.1:c.2828-476T>G	XP_011537897.1:n.2828-476T>G
XM_011539596.1:c.2756-476T>G	XP_011537898.1:n.2756-476T>G
XM_011539597.1:c.2675-476T>G	XP_011537899.1:n.2675-476T>G
XM_011539592.3:c.3038-476T>G	XP_011537894.1:n.3038-476T>G
XM_011539593.3:c.3014-476T>G	XP_011537895.1:n.3014-476T>G
XM_011539594.2:c.2828-476T>G	XP_011537896.1:n.2828-476T>G
XM_011539595.2:c.2828-476T>G	XP_011537897.1:n.2828-476T>G
XM_011539596.2:c.2756-476T>G	XP_011537898.1:n.2756-476T>G
XM_011539597.3:c.2675-476T>G	XP_011537899.1:n.2675-476T>G
XM_017016041.2:c.2603-476T>G	XP_016871530.1:n.2603-476T>G
XM_024447927.1:c.3038-476T>G	XP_024303695.1:n.3038-476T>G
XM_024447928.1:c.3038-476T>G	XP_024303696.1:n.3038-476T>G
XM_024447929.1:c.2966-476T>G	XP_024303697.1:n.2966-476T>G
XM_024447930.1:c.2966-476T>G	XP_024303698.1:n.2966-476T>G
XM_024447931.1:c.2942-476T>G	XP_024303699.1:n.2942-476T>G
XM_024447932.1:c.1421-476T>G	XP_024303700.1:n.1421-476T>G
NM_001278185.2:c.2732-476T>G	NP_001265114.1:n.2732-476T>G
NM_001278186.2:c.2177-476T>G	NP_001265115.1:n.2177-476T>G
NM_015601.4:c.2942-476T>G MANE Select	NP_056416.2:n.2942-476T>G
NM_022079.3:c.2966-476T>G	NP_071362.1:n.2966-476T>G