Canonical Allele Identifier: CA1445223317

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144902_25144903delinsTG , CM000666.2:g.25144902_25144903delinsTG	GRCh38
NC_000004.11:g.25146524_25146525delinsTG , CM000666.1:g.25146524_25146525delinsTG	GRCh37
NC_000004.10:g.24755622_24755623delinsTG	NCBI36
NG_028222.1:g.20680_20681delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.935-38_935-37delinsCA MANE Select	ENSP00000371535.2:n.935-38_935-37delinsCA
ENST00000680581.1:c.935-38_935-37delinsCA	ENSP00000506483.1:n.935-38_935-37delinsCA
ENST00000680824.1:n.2151-38_2151-37delinsCA
ENST00000681071.1:n.1227-38_1227-37delinsCA
ENST00000681341.1:n.2076-38_2076-37delinsCA
ENST00000681948.1:c.1190-38_1190-37delinsCA	ENSP00000505991.1:n.1190-38_1190-37delinsCA
ENST00000358971.7:c.*733-38_*733-37delinsCA	ENSP00000351857.3:n.*733-38_*733-37delinsCA
ENST00000382103.6:c.935-38_935-37delinsCA	ENSP00000371535.2:n.935-38_935-37delinsCA
ENST00000503150.1:c.217-38_217-37delinsCA
ENST00000505513.1:n.235-38_235-37delinsCA
ENST00000514585.5:c.*636-38_*636-37delinsCA	ENSP00000421880.1:n.*636-38_*636-37delinsCA
NM_016955.3:c.935-38_935-37delinsCA	NP_058651.3:n.935-38_935-37delinsCA
XM_005248168.2:c.698-38_698-37delinsCA	XP_005248225.1:n.698-38_698-37delinsCA
XM_006713965.2:c.755-38_755-37delinsCA	XP_006714028.1:n.755-38_755-37delinsCA
XM_011513846.1:c.932-38_932-37delinsCA	XP_011512148.1:n.932-38_932-37delinsCA
XM_011513847.1:c.902-38_902-37delinsCA	XP_011512149.1:n.902-38_902-37delinsCA
XM_011513848.1:c.755-38_755-37delinsCA	XP_011512150.1:n.755-38_755-37delinsCA
XM_011513846.2:c.932-38_932-37delinsCA	XP_011512148.1:n.932-38_932-37delinsCA
XM_011513847.2:c.902-38_902-37delinsCA	XP_011512149.1:n.902-38_902-37delinsCA
XM_017008277.1:c.1190-38_1190-37delinsCA	XP_016863766.1:n.1190-38_1190-37delinsCA
XM_017008278.1:c.512-38_512-37delinsCA	XP_016863767.1:n.512-38_512-37delinsCA
NM_016955.4:c.935-38_935-37delinsCA MANE Select	NP_058651.3:n.935-38_935-37delinsCA