Canonical Allele Identifier: CA2573130182
Gene: FOXA1 HGNC NCBI
TTC6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37594962_37594967del , CM000676.2:g.37594962_37594967del GRCh38
NC_000014.8:g.38064167_38064172del , CM000676.1:g.38064167_38064172del GRCh37
NC_000014.7:g.37133918_37133923del NCBI36
NG_033028.1:g.5154_5159del

Transcript Alleles

HGVS Amino-acid Change
ENST00000250448.5:c.6_11del (FOXA1) MANE Select ENSP00000250448.3:p.Leu2_Thr4delinsPhe
ENST00000250448.2:c.6_11del (FOXA1) ENSP00000250448.2:p.Leu2_Thr4delinsPhe
ENST00000553751.1:c.6_11del (FOXA1) ENSP00000451704.1:p.Leu2_Thr4delinsPhe
NM_004496.3:c.6_11del (FOXA1) NP_004487.2:p.Leu2_Thr4delinsPhe
XM_024449560.1:c.-308+1408_-308+1413del (TTC6) XP_024305328.1:n.-308+1408_-308+1413del
NM_004496.4:c.6_11del (FOXA1) NP_004487.2:p.Leu2_Thr4delinsPhe
NM_004496.5:c.6_11del (FOXA1) MANE Select NP_004487.2:p.Leu2_Thr4delinsPhe
Search 100 bp 5'
Search 100 bp 3'