Canonical Allele Identifier: CA2877304
Gene: SEPSECS HGNC NCBI

Linked Data

dbSNP Id: rs191720294
gnomAD v2: 4-25146525-G-T
gnomAD v3: 4-25144903-G-T
gnomAD v4: 4-25144903-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144903G>T , CM000666.2:g.25144903G>T GRCh38
NC_000004.11:g.25146525G>T , CM000666.1:g.25146525G>T GRCh37
NC_000004.10:g.24755623G>T NCBI36
NG_028222.1:g.20680C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.935-38C>A MANE Select ENSP00000371535.2:n.935-38C>A
ENST00000680581.1:c.935-38C>A ENSP00000506483.1:n.935-38C>A
ENST00000680824.1:n.2151-38C>A
ENST00000681071.1:n.1227-38C>A
ENST00000681341.1:n.2076-38C>A
ENST00000681948.1:c.1190-38C>A ENSP00000505991.1:n.1190-38C>A
ENST00000358971.7:c.*733-38C>A ENSP00000351857.3:n.*733-38C>A
ENST00000382103.6:c.935-38C>A ENSP00000371535.2:n.935-38C>A
ENST00000503150.1:c.217-38C>A
ENST00000505513.1:n.235-38C>A
ENST00000514585.5:c.*636-38C>A ENSP00000421880.1:n.*636-38C>A
NM_016955.3:c.935-38C>A NP_058651.3:n.935-38C>A
XM_005248168.2:c.698-38C>A XP_005248225.1:n.698-38C>A
XM_006713965.2:c.755-38C>A XP_006714028.1:n.755-38C>A
XM_011513846.1:c.932-38C>A XP_011512148.1:n.932-38C>A
XM_011513847.1:c.902-38C>A XP_011512149.1:n.902-38C>A
XM_011513848.1:c.755-38C>A XP_011512150.1:n.755-38C>A
XM_011513846.2:c.932-38C>A XP_011512148.1:n.932-38C>A
XM_011513847.2:c.902-38C>A XP_011512149.1:n.902-38C>A
XM_017008277.1:c.1190-38C>A XP_016863766.1:n.1190-38C>A
XM_017008278.1:c.512-38C>A XP_016863767.1:n.512-38C>A
NM_016955.4:c.935-38C>A MANE Select NP_058651.3:n.935-38C>A