Canonical Allele Identifier: CA1445208213

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156705_25156712delinsCTCAAAAA , CM000666.2:g.25156705_25156712delinsCTCAAAAA	GRCh38
NC_000004.11:g.25158327_25158334delinsCTCAAAAA , CM000666.1:g.25158327_25158334delinsCTCAAAAA	GRCh37
NC_000004.10:g.24767425_24767432delinsCTCAAAAA	NCBI36
NG_028222.1:g.8871_8878delinsTTTTTGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+144_388+151delinsTTTTTGAG MANE Select	ENSP00000371535.2:n.388+144_388+151delins...
ENST00000680581.1:c.388+144_388+151delinsTTTTTGAG	ENSP00000506483.1:n.388+144_388+151delins...
ENST00000680824.1:n.1604+144_1604+151delinsTTTTTGAG
ENST00000681071.1:n.680+144_680+151delinsTTTTTGAG
ENST00000681166.1:n.1435+144_1435+151delinsTTTTTGAG
ENST00000681341.1:n.1529+144_1529+151delinsTTTTTGAG
ENST00000681640.1:n.482+144_482+151delinsTTTTTGAG
ENST00000681948.1:c.643+144_643+151delinsTTTTTGAG	ENSP00000505991.1:n.643+144_643+151delins...
ENST00000358971.7:c.*186+144_*186+151delinsTTTTTGAG	ENSP00000351857.3:n.*186+144_*186+151deli...
ENST00000382103.6:c.388+144_388+151delinsTTTTTGAG	ENSP00000371535.2:n.388+144_388+151delins...
ENST00000514585.5:c.*89+144_*89+151delinsTTTTTGAG	ENSP00000421880.1:n.*89+144_*89+151delins...
NM_016955.3:c.388+144_388+151delinsTTTTTGAG	NP_058651.3:n.388+144_388+151delinsTTTTTG...
XM_005248168.2:c.151+144_151+151delinsTTTTTGAG	XP_005248225.1:n.151+144_151+151delinsTTT...
XM_006713965.2:c.208+144_208+151delinsTTTTTGAG	XP_006714028.1:n.208+144_208+151delinsTTT...
XM_011513846.1:c.385+144_385+151delinsTTTTTGAG	XP_011512148.1:n.385+144_385+151delinsTTT...
XM_011513847.1:c.355+144_355+151delinsTTTTTGAG	XP_011512149.1:n.355+144_355+151delinsTTT...
XM_011513848.1:c.208+144_208+151delinsTTTTTGAG	XP_011512150.1:n.208+144_208+151delinsTTT...
XM_011513846.2:c.385+144_385+151delinsTTTTTGAG	XP_011512148.1:n.385+144_385+151delinsTTT...
XM_011513847.2:c.355+144_355+151delinsTTTTTGAG	XP_011512149.1:n.355+144_355+151delinsTTT...
XM_017008277.1:c.643+144_643+151delinsTTTTTGAG	XP_016863766.1:n.643+144_643+151delinsTTT...
XM_017008278.1:c.-36+144_-36+151delinsTTTTTGAG	XP_016863767.1:n.-36+144_-36+151delinsTTT...
NM_016955.4:c.388+144_388+151delinsTTTTTGAG MANE Select	NP_058651.3:n.388+144_388+151delinsTTTTTG...