Canonical Allele Identifier: CA2638191139
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254457_44254458insGCC , CM000679.2:g.44254457_44254458insGCC GRCh38
NC_000017.10:g.42331825_42331826insGCC , CM000679.1:g.42331825_42331826insGCC GRCh37
NC_000017.9:g.39687351_39687352insGCC NCBI36
NG_007498.1:g.18677_18678insGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.2057+38_2057+39insGGC MANE Select ENSP00000262418.6:n.2057+38_2057+39insGGC
ENST00000262418.10:c.2057+38_2057+39insGGC ENSP00000262418.6:n.2057+38_2057+39insGGC
ENST00000399246.3:c.959+38_959+39insGGC ENSP00000382190.3:n.959+38_959+39insGGC
NM_000342.3:c.2057+38_2057+39insGGC NP_000333.1:n.2057+38_2057+39insGGC
XM_005257593.3:c.1862+38_1862+39insGGC XP_005257650.1:n.1862+38_1862+39insGGC
XM_011525129.1:c.1967+38_1967+39insGGC XP_011523431.1:n.1967+38_1967+39insGGC
XM_011525130.1:c.2057+38_2057+39insGGC XP_011523432.1:n.2057+38_2057+39insGGC
XM_011525131.1:c.2057+38_2057+39insGGC XP_011523433.1:n.2057+38_2057+39insGGC
XM_005257593.5:c.1862+38_1862+39insGGC XP_005257650.1:n.1862+38_1862+39insGGC
XM_011525129.2:c.1967+38_1967+39insGGC XP_011523431.1:n.1967+38_1967+39insGGC
NM_000342.4:c.2057+38_2057+39insGGC MANE Select NP_000333.1:n.2057+38_2057+39insGGC