Canonical Allele Identifier: CA1072491858
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v3: 5-1212961-CA-C
gnomAD v4: 5-1212961-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212962del , CM000667.2:g.1212962del GRCh38
NC_000005.9:g.1213077del , CM000667.1:g.1213077del GRCh37
NC_000005.8:g.1266077del NCBI36
NG_008282.1:g.16368del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.663+478del MANE Select ENSP00000305302.10:n.663+478del
ENST00000304460.10:c.663+478del ENSP00000305302.10:n.663+478del
ENST00000515652.5:c.571+478del ENSP00000425701.1:n.571+478del
NM_001003841.2:c.663+478del NP_001003841.1:n.663+478del
NM_001003841.3:c.663+478del MANE Select NP_001003841.1:n.663+478del
Search 100 bp 5'
Search 100 bp 3'