Canonical Allele Identifier: CA2877301

Gene: SEPSECS

Linked Data

• dbSNP Id: rs769755395
• ExAC: 4:25146524 T / TG
• gnomAD v2: 4-25146524-T-TG
• gnomAD v3: 4-25144902-T-TG
• gnomAD v4: 4-25144902-T-TG
• MyVariant Identifiers: chr4:g.25146525_25146526insG (hg19) ; chr4:g.25146524_25146525insG (hg19) ; chr4:g.25144903_25144904insG (hg38) ; chr4:g.25144902_25144903insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144909dup , CM000666.2:g.25144909dup	GRCh38
NC_000004.11:g.25146531dup , CM000666.1:g.25146531dup	GRCh37
NC_000004.10:g.24755629dup	NCBI36
NG_028222.1:g.20680dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.935-38dup MANE Select	ENSP00000371535.2:n.935-38dup
ENST00000680581.1:c.935-38dup	ENSP00000506483.1:n.935-38dup
ENST00000680824.1:n.2151-38dup
ENST00000681071.1:n.1227-38dup
ENST00000681341.1:n.2076-38dup
ENST00000681948.1:c.1190-38dup	ENSP00000505991.1:n.1190-38dup
ENST00000358971.7:c.*733-38dup	ENSP00000351857.3:n.*733-38dup
ENST00000382103.6:c.935-38dup	ENSP00000371535.2:n.935-38dup
ENST00000503150.1:c.217-38dup
ENST00000505513.1:n.235-38dup
ENST00000514585.5:c.*636-38dup	ENSP00000421880.1:n.*636-38dup
NM_016955.3:c.935-38dup	NP_058651.3:n.935-38dup
XM_005248168.2:c.698-38dup	XP_005248225.1:n.698-38dup
XM_006713965.2:c.755-38dup	XP_006714028.1:n.755-38dup
XM_011513846.1:c.932-38dup	XP_011512148.1:n.932-38dup
XM_011513847.1:c.902-38dup	XP_011512149.1:n.902-38dup
XM_011513848.1:c.755-38dup	XP_011512150.1:n.755-38dup
XM_011513846.2:c.932-38dup	XP_011512148.1:n.932-38dup
XM_011513847.2:c.902-38dup	XP_011512149.1:n.902-38dup
XM_017008277.1:c.1190-38dup	XP_016863766.1:n.1190-38dup
XM_017008278.1:c.512-38dup	XP_016863767.1:n.512-38dup
NM_016955.4:c.935-38dup MANE Select	NP_058651.3:n.935-38dup