Canonical Allele Identifier: CA1445538104
Gene: SEL1L3 HGNC NCBI

Linked Data

dbSNP Id: rs1713756449

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25808510C>G , CM000666.2:g.25808510C>G GRCh38
NC_000004.11:g.25810132C>G , CM000666.1:g.25810132C>G GRCh37
NC_000004.10:g.25419230C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399878.8:c.1565-3758G>C MANE Select ENSP00000382767.3:n.1565-3758G>C
ENST00000264868.9:c.1460-3758G>C ENSP00000264868.5:n.1460-3758G>C
ENST00000399878.7:c.1565-3758G>C ENSP00000382767.3:n.1565-3758G>C
ENST00000502949.5:c.1106-3758G>C ENSP00000425438.1:n.1106-3758G>C
NM_001297592.1:c.1460-3758G>C NP_001284521.1:n.1460-3758G>C
NM_001297594.1:c.1106-3758G>C NP_001284523.1:n.1106-3758G>C
NM_015187.4:c.1565-3758G>C NP_056002.2:n.1565-3758G>C
XM_011513818.1:c.1106-3758G>C XP_011512120.1:n.1106-3758G>C
XM_011513819.1:c.1106-3758G>C XP_011512121.1:n.1106-3758G>C
XM_011513820.1:c.1106-3758G>C XP_011512122.1:n.1106-3758G>C
XM_011513819.2:c.1565-3758G>C XP_011512121.2:n.1565-3758G>C
XM_024453953.1:c.1106-3758G>C XP_024309721.1:n.1106-3758G>C
XM_024453954.1:c.1106-3758G>C XP_024309722.1:n.1106-3758G>C
XM_024453955.1:c.1106-3758G>C XP_024309723.1:n.1106-3758G>C
XR_001741182.2:n.1507-3758G>C
NM_015187.5:c.1565-3758G>C MANE Select NP_056002.2:n.1565-3758G>C
NM_001297592.2:c.1460-3758G>C NP_001284521.1:n.1460-3758G>C
NM_001297594.2:c.1106-3758G>C NP_001284523.1:n.1106-3758G>C