Canonical Allele Identifier: CA1445208679

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156858G= , CM000666.2:g.25156858G=	GRCh38
NC_000004.11:g.25158480G= , CM000666.1:g.25158480G=	GRCh37
NC_000004.10:g.24767578G=	NCBI36
NG_028222.1:g.8725C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.386C= MANE Select	ENSP00000371535.2:p.Ala129=
ENST00000680581.1:c.386C=	ENSP00000506483.1:p.Ala129=
ENST00000680824.1:n.1602C=
ENST00000681071.1:n.678C=
ENST00000681166.1:n.1433C=
ENST00000681341.1:n.1527C=
ENST00000681640.1:n.480C=
ENST00000681948.1:c.641C=	ENSP00000505991.1:p.Ala214=
ENST00000358971.7:c.*184C=	ENSP00000351857.3:n.*184C=
ENST00000382103.6:c.386C=	ENSP00000371535.2:p.Ala129=
ENST00000514585.5:c.*87C=	ENSP00000421880.1:n.*87C=
NM_016955.3:c.386C=	NP_058651.3:p.Ala129=
XM_005248168.2:c.149C=	XP_005248225.1:p.Ala50=
XM_006713965.2:c.206C=	XP_006714028.1:p.Ala69=
XM_011513846.1:c.383C=	XP_011512148.1:p.Ala128=
XM_011513847.1:c.353C=	XP_011512149.1:p.Ala118=
XM_011513848.1:c.206C=	XP_011512150.1:p.Ala69=
XM_011513846.2:c.383C=	XP_011512148.1:p.Ala128=
XM_011513847.2:c.353C=	XP_011512149.1:p.Ala118=
XM_017008277.1:c.641C=	XP_016863766.1:p.Ala214=
XM_017008278.1:c.-38C=	XP_016863767.1:n.-38C=
NM_016955.4:c.386C= MANE Select	NP_058651.3:p.Ala129=