Canonical Allele Identifier: CA438732711

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158505A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156883A>G , CM000666.2:g.25156883A>G	GRCh38
NC_000004.11:g.25158505A>G , CM000666.1:g.25158505A>G	GRCh37
NC_000004.10:g.24767603A>G	NCBI36
NG_028222.1:g.8700T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.361T>C MANE Select	ENSP00000371535.2:p.Leu121=
ENST00000680581.1:c.361T>C	ENSP00000506483.1:p.Leu121=
ENST00000680824.1:n.1577T>C
ENST00000681071.1:n.653T>C
ENST00000681166.1:n.1408T>C
ENST00000681341.1:n.1502T>C
ENST00000681640.1:n.455T>C
ENST00000681948.1:c.616T>C	ENSP00000505991.1:p.Leu206=
ENST00000358971.7:c.*159T>C	ENSP00000351857.3:n.*159T>C
ENST00000382103.6:c.361T>C	ENSP00000371535.2:p.Leu121=
ENST00000514585.5:c.*62T>C	ENSP00000421880.1:n.*62T>C
NM_016955.3:c.361T>C	NP_058651.3:p.Leu121=
XM_005248168.2:c.124T>C	XP_005248225.1:p.Leu42=
XM_006713965.2:c.181T>C	XP_006714028.1:p.Leu61=
XM_011513846.1:c.358T>C	XP_011512148.1:p.Leu120=
XM_011513847.1:c.328T>C	XP_011512149.1:p.Leu110=
XM_011513848.1:c.181T>C	XP_011512150.1:p.Leu61=
XM_011513846.2:c.358T>C	XP_011512148.1:p.Leu120=
XM_011513847.2:c.328T>C	XP_011512149.1:p.Leu110=
XM_017008277.1:c.616T>C	XP_016863766.1:p.Leu206=
XM_017008278.1:c.-63T>C	XP_016863767.1:n.-63T>C
NM_016955.4:c.361T>C MANE Select	NP_058651.3:p.Leu121=