Canonical Allele Identifier: CA1060322868
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144266_25144267insCT , CM000666.2:g.25144266_25144267insCT GRCh38
NC_000004.11:g.25145888_25145889insCT , CM000666.1:g.25145888_25145889insCT GRCh37
NC_000004.10:g.24754986_24754987insCT NCBI36
NG_028222.1:g.21316_21317insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+507_1026+508insAG MANE Select ENSP00000371535.2:n.1026+507_1026+508insAG
ENST00000680581.1:c.1026+507_1026+508insAG ENSP00000506483.1:n.1026+507_1026+508insAG
ENST00000680824.1:n.2242+507_2242+508insAG
ENST00000681071.1:n.1318+507_1318+508insAG
ENST00000681341.1:n.2167+507_2167+508insAG
ENST00000681948.1:c.1281+507_1281+508insAG ENSP00000505991.1:n.1281+507_1281+508insAG
ENST00000358971.7:c.*824+507_*824+508insAG ENSP00000351857.3:n.*824+507_*824+508insAG
ENST00000382103.6:c.1026+507_1026+508insAG ENSP00000371535.2:n.1026+507_1026+508insAG
ENST00000503150.1:c.308+507_308+508insAG
ENST00000505513.1:n.326+507_326+508insAG
ENST00000514585.5:c.*727+507_*727+508insAG ENSP00000421880.1:n.*727+507_*727+508insAG
NM_016955.3:c.1026+507_1026+508insAG NP_058651.3:n.1026+507_1026+508insAG
XM_005248168.2:c.789+507_789+508insAG XP_005248225.1:n.789+507_789+508insAG
XM_006713965.2:c.846+507_846+508insAG XP_006714028.1:n.846+507_846+508insAG
XM_011513846.1:c.1023+507_1023+508insAG XP_011512148.1:n.1023+507_1023+508insAG
XM_011513847.1:c.993+507_993+508insAG XP_011512149.1:n.993+507_993+508insAG
XM_011513848.1:c.846+507_846+508insAG XP_011512150.1:n.846+507_846+508insAG
XM_011513846.2:c.1023+507_1023+508insAG XP_011512148.1:n.1023+507_1023+508insAG
XM_011513847.2:c.993+507_993+508insAG XP_011512149.1:n.993+507_993+508insAG
XM_017008277.1:c.1281+507_1281+508insAG XP_016863766.1:n.1281+507_1281+508insAG
XM_017008278.1:c.603+507_603+508insAG XP_016863767.1:n.603+507_603+508insAG
NM_016955.4:c.1026+507_1026+508insAG MANE Select NP_058651.3:n.1026+507_1026+508insAG