Canonical Allele Identifier: CA2670197230

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156784-TAAATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156791_25156795del , CM000666.2:g.25156791_25156795del	GRCh38
NC_000004.11:g.25158413_25158417del , CM000666.1:g.25158413_25158417del	GRCh37
NC_000004.10:g.24767511_24767515del	NCBI36
NG_028222.1:g.8794_8798del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+67_388+71del MANE Select	ENSP00000371535.2:n.388+67_388+71del
ENST00000680581.1:c.388+67_388+71del	ENSP00000506483.1:n.388+67_388+71del
ENST00000680824.1:n.1604+67_1604+71del
ENST00000681071.1:n.680+67_680+71del
ENST00000681166.1:n.1435+67_1435+71del
ENST00000681341.1:n.1529+67_1529+71del
ENST00000681640.1:n.482+67_482+71del
ENST00000681948.1:c.643+67_643+71del	ENSP00000505991.1:n.643+67_643+71del
ENST00000358971.7:c.*186+67_*186+71del	ENSP00000351857.3:n.*186+67_*186+71del
ENST00000382103.6:c.388+67_388+71del	ENSP00000371535.2:n.388+67_388+71del
ENST00000514585.5:c.*89+67_*89+71del	ENSP00000421880.1:n.*89+67_*89+71del
NM_016955.3:c.388+67_388+71del	NP_058651.3:n.388+67_388+71del
XM_005248168.2:c.151+67_151+71del	XP_005248225.1:n.151+67_151+71del
XM_006713965.2:c.208+67_208+71del	XP_006714028.1:n.208+67_208+71del
XM_011513846.1:c.385+67_385+71del	XP_011512148.1:n.385+67_385+71del
XM_011513847.1:c.355+67_355+71del	XP_011512149.1:n.355+67_355+71del
XM_011513848.1:c.208+67_208+71del	XP_011512150.1:n.208+67_208+71del
XM_011513846.2:c.385+67_385+71del	XP_011512148.1:n.385+67_385+71del
XM_011513847.2:c.355+67_355+71del	XP_011512149.1:n.355+67_355+71del
XM_017008277.1:c.643+67_643+71del	XP_016863766.1:n.643+67_643+71del
XM_017008278.1:c.-36+67_-36+71del	XP_016863767.1:n.-36+67_-36+71del
NM_016955.4:c.388+67_388+71del MANE Select	NP_058651.3:n.388+67_388+71del