Canonical Allele Identifier: CA2638191189
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254461_44254462insAC , CM000679.2:g.44254461_44254462insAC GRCh38
NC_000017.10:g.42331829_42331830insAC , CM000679.1:g.42331829_42331830insAC GRCh37
NC_000017.9:g.39687355_39687356insAC NCBI36
NG_007498.1:g.18673_18674insGT

Transcript Alleles

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