Canonical Allele Identifier: CA6875191
Gene: SLC15A4 HGNC NCBI

Linked Data

dbSNP Id: rs753096233
ExAC: 12:129299611 TTAACCTAAAA / T
gnomAD v2: 12-129299611-TTAACCTAAAA-T
gnomAD v3: 12-128815066-TTAACCTAAAA-T
gnomAD v4: 12-128815066-TTAACCTAAAA-T
MyVariant Identifiers: chr12:g.129299612_129299621del (hg19) chr12:g.128815067_128815076del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128815071_128815080del , CM000674.2:g.128815071_128815080del GRCh38
NC_000012.11:g.129299616_129299625del , CM000674.1:g.129299616_129299625del GRCh37
NC_000012.10:g.127865569_127865578del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.547-6_550del
ENST00000266771.9:c.547-6_550del
ENST00000366292.6:n.853_862del
ENST00000376740.8:c.126-6_129del
ENST00000376744.8:c.383-6_386del
ENST00000535272.1:n.341-6_344del
ENST00000539703.1:n.197-6_200del
NM_145648.3:c.547-6_550del
XM_011537895.1:c.697-6_700del
XR_429081.2:n.570-6_573del
XR_944494.1:n.720-6_723del
XR_944495.1:n.720-6_723del
XR_944496.1:n.720-6_723del
XR_944497.1:n.720-6_723del
XM_017018791.1:c.697-6_700del
XM_017018792.1:c.697-6_700del
XM_017018793.1:c.547-6_550del
XR_002957287.1:n.570-6_573del
XR_944496.2:n.720-6_723del
NM_145648.4:c.547-6_550del
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