Canonical Allele Identifier: CA356542553

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158487T>G (hg19) ; chr4:g.25156865T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156865T>G , CM000666.2:g.25156865T>G	GRCh38
NC_000004.11:g.25158487T>G , CM000666.1:g.25158487T>G	GRCh37
NC_000004.10:g.24767585T>G	NCBI36
NG_028222.1:g.8718A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.379A>C MANE Select	ENSP00000371535.2:p.Lys127Gln
ENST00000680581.1:c.379A>C	ENSP00000506483.1:p.Lys127Gln
ENST00000680824.1:n.1595A>C
ENST00000681071.1:n.671A>C
ENST00000681166.1:n.1426A>C
ENST00000681341.1:n.1520A>C
ENST00000681640.1:n.473A>C
ENST00000681948.1:c.634A>C	ENSP00000505991.1:p.Lys212Gln
ENST00000358971.7:c.*177A>C	ENSP00000351857.3:n.*177A>C
ENST00000382103.6:c.379A>C	ENSP00000371535.2:p.Lys127Gln
ENST00000514585.5:c.*80A>C	ENSP00000421880.1:n.*80A>C
NM_016955.3:c.379A>C	NP_058651.3:p.Lys127Gln
XM_005248168.2:c.142A>C	XP_005248225.1:p.Lys48Gln
XM_006713965.2:c.199A>C	XP_006714028.1:p.Lys67Gln
XM_011513846.1:c.376A>C	XP_011512148.1:p.Lys126Gln
XM_011513847.1:c.346A>C	XP_011512149.1:p.Lys116Gln
XM_011513848.1:c.199A>C	XP_011512150.1:p.Lys67Gln
XM_011513846.2:c.376A>C	XP_011512148.1:p.Lys126Gln
XM_011513847.2:c.346A>C	XP_011512149.1:p.Lys116Gln
XM_017008277.1:c.634A>C	XP_016863766.1:p.Lys212Gln
XM_017008278.1:c.-45A>C	XP_016863767.1:n.-45A>C
NM_016955.4:c.379A>C MANE Select	NP_058651.3:p.Lys127Gln