Canonical Allele Identifier: CA2638191188
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254464_44254465insACCCCCGGCCCCCCCCCCC , CM000679.2:g.44254464_44254465insACCCCCGGCCCCCCCCCCC GRCh38
NC_000017.10:g.42331832_42331833insACCCCCGGCCCCCCCCCCC , CM000679.1:g.42331832_42331833insACCCCCGGCCCCCCCCCCC GRCh37
NC_000017.9:g.39687358_39687359insACCCCCGGCCCCCCCCCCC NCBI36
NG_007498.1:g.18673_18674insGGGGGGGGCCGGGGGTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG MANE Select ENSP00000262418.6:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG
ENST00000262418.10:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG ENSP00000262418.6:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG
ENST00000399246.3:c.959+34_959+35insGGGGGGGGCCGGGGGTGGG ENSP00000382190.3:n.959+34_959+35insGGGGGGGGCCGGGGGTGGG
NM_000342.3:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG NP_000333.1:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG
XM_005257593.3:c.1862+34_1862+35insGGGGGGGGCCGGGGGTGGG XP_005257650.1:n.1862+34_1862+35insGGGGGGGGCCGGGGGTGGG
XM_011525129.1:c.1967+34_1967+35insGGGGGGGGCCGGGGGTGGG XP_011523431.1:n.1967+34_1967+35insGGGGGGGGCCGGGGGTGGG
XM_011525130.1:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG XP_011523432.1:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG
XM_011525131.1:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG XP_011523433.1:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG
XM_005257593.5:c.1862+34_1862+35insGGGGGGGGCCGGGGGTGGG XP_005257650.1:n.1862+34_1862+35insGGGGGGGGCCGGGGGTGGG
XM_011525129.2:c.1967+34_1967+35insGGGGGGGGCCGGGGGTGGG XP_011523431.1:n.1967+34_1967+35insGGGGGGGGCCGGGGGTGGG
NM_000342.4:c.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG MANE Select NP_000333.1:n.2057+34_2057+35insGGGGGGGGCCGGGGGTGGG