Canonical Allele Identifier: CA108174806
Gene: SLC10A7 HGNC NCBI

Linked Data

dbSNP Id: rs191493117
gnomAD v2: 4-147360131-C-T
gnomAD v3: 4-146438979-C-T
gnomAD v4: 4-146438979-C-T
MyVariant Identifiers: chr4:g.147360131C>T (hg19) chr4:g.146438979C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.146438979C>T , CM000666.2:g.146438979C>T GRCh38
NC_000004.11:g.147360131C>T , CM000666.1:g.147360131C>T GRCh37
NC_000004.10:g.147579581C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000511315.2:n.272+3804G>A
ENST00000685433.1:n.1090+3804G>A
ENST00000693222.1:c.525+3804G>A ENSP00000508969.1:n.525+3804G>A
ENST00000335472.12:c.435+3804G>A MANE Select ENSP00000334594.8:n.435+3804G>A
ENST00000335472.11:c.435+3804G>A ENSP00000334594.7:n.435+3804G>A
ENST00000432059.6:c.396+64870G>A ENSP00000411297.2:n.396+64870G>A
ENST00000507030.5:c.435+3804G>A ENSP00000421275.1:n.435+3804G>A
ENST00000507560.5:n.378+3804G>A
NM_001029998.4:c.435+3804G>A NP_001025169.1:n.435+3804G>A
NM_001300842.1:c.435+3804G>A NP_001287771.1:n.435+3804G>A
XM_011532311.1:c.396+64870G>A XP_011530613.1:n.396+64870G>A
XM_011532312.1:c.396+64870G>A XP_011530614.1:n.396+64870G>A
XM_011532313.1:c.96+3804G>A XP_011530615.1:n.96+3804G>A
XR_938780.1:n.689+3804G>A
NM_001029998.5:c.435+3804G>A NP_001025169.1:n.435+3804G>A
NM_001300842.2:c.435+3804G>A NP_001287771.1:n.435+3804G>A
NM_001317816.1:c.396+64870G>A NP_001304745.1:n.396+64870G>A
NR_133924.1:n.689+3804G>A
XM_011532311.2:c.396+64870G>A XP_011530613.1:n.396+64870G>A
XM_011532313.2:c.96+3804G>A XP_011530615.1:n.96+3804G>A
XM_017008690.2:c.435+3804G>A XP_016864179.1:n.435+3804G>A
XM_017008692.1:c.*1+64870G>A XP_016864181.1:n.*1+64870G>A
XR_001741332.2:n.661+3804G>A
XR_001741333.1:n.579+3804G>A
XR_938780.3:n.661+3804G>A
NM_001029998.6:c.435+3804G>A MANE Select NP_001025169.1:n.435+3804G>A
NM_001300842.3:c.435+3804G>A NP_001287771.1:n.435+3804G>A
NM_001317816.2:c.396+64870G>A NP_001304745.1:n.396+64870G>A
NR_133924.2:n.658+3804G>A
Search 100 bp 5'
Search 100 bp 3'