Canonical Allele Identifier: CA399784091
Community Standard Title: NM_000342.4(SLC4A1):c.1765C>G (p.Arg589Gly)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44255708G>C , CM000679.2:g.44255708G>C GRCh38
NC_000017.10:g.42333076G>C , CM000679.1:g.42333076G>C GRCh37
NC_000017.9:g.39688602G>C NCBI36
NG_007498.1:g.17427C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.1765C>G MANE Select NP_000333.1:p.Arg589Gly
ENST00000262418.12:c.1765C>G MANE Select ENSP00000262418.6:p.Arg589Gly
NM_000342.3:c.1765C>G NP_000333.1:p.Arg589Gly
ENST00000262418.10:c.1765C>G ENSP00000262418.6:p.Arg589Gly
ENST00000399246.3:c.778-487C>G ENSP00000382190.3:n.778-487C>G
XM_005257593.3:c.1570C>G XP_005257650.1:p.Arg524Gly
XM_005257593.5:c.1570C>G XP_005257650.1:p.Arg524Gly
XM_011525129.1:c.1765C>G XP_011523431.1:p.Arg589Gly
XM_011525129.2:c.1765C>G XP_011523431.1:p.Arg589Gly
XM_011525130.1:c.1765C>G XP_011523432.1:p.Arg589Gly
XM_011525131.1:c.1765C>G XP_011523433.1:p.Arg589Gly