Canonical Allele Identifier: CA2760775169

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156979G>A , CM000666.2:g.25156979G>A	GRCh38
NC_000004.11:g.25158601G>A , CM000666.1:g.25158601G>A	GRCh37
NC_000004.10:g.24767699G>A	NCBI36
NG_028222.1:g.8604C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.270-5C>T MANE Select	ENSP00000371535.2:n.270-5C>T
ENST00000680581.1:c.270-5C>T	ENSP00000506483.1:n.270-5C>T
ENST00000680824.1:n.1486-5C>T
ENST00000681071.1:n.557C>T
ENST00000681166.1:n.1317-5C>T
ENST00000681341.1:n.1411-5C>T
ENST00000681640.1:n.364-5C>T
ENST00000681948.1:c.525-5C>T	ENSP00000505991.1:n.525-5C>T
ENST00000358971.7:c.*68-5C>T	ENSP00000351857.3:n.*68-5C>T
ENST00000382103.6:c.270-5C>T	ENSP00000371535.2:n.270-5C>T
ENST00000514585.5:c.115-5C>T	ENSP00000421880.1:n.115-5C>T
NM_016955.3:c.270-5C>T	NP_058651.3:n.270-5C>T
XM_005248168.2:c.33-5C>T	XP_005248225.1:n.33-5C>T
XM_006713965.2:c.90-5C>T	XP_006714028.1:n.90-5C>T
XM_011513846.1:c.267-5C>T	XP_011512148.1:n.267-5C>T
XM_011513847.1:c.237-5C>T	XP_011512149.1:n.237-5C>T
XM_011513848.1:c.90-5C>T	XP_011512150.1:n.90-5C>T
XM_011513846.2:c.267-5C>T	XP_011512148.1:n.267-5C>T
XM_011513847.2:c.237-5C>T	XP_011512149.1:n.237-5C>T
XM_017008277.1:c.525-5C>T	XP_016863766.1:n.525-5C>T
XM_017008278.1:c.-159C>T	XP_016863767.1:n.-159C>T
NM_016955.4:c.270-5C>T MANE Select	NP_058651.3:n.270-5C>T