Canonical Allele Identifier: CA2261309580
Community Standard Title: NM_000342.4(SLC4A1):c.1438G= (p.Glu480=)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44257538C= , CM000679.2:g.44257538C= GRCh38
NC_000017.10:g.42334906C= , CM000679.1:g.42334906C= GRCh37
NC_000017.9:g.39690432C= NCBI36
NG_007498.1:g.15597G=

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.1438G= MANE Select NP_000333.1:p.Glu480=
ENST00000262418.12:c.1438G= MANE Select ENSP00000262418.6:p.Glu480=
NM_000342.3:c.1438G= NP_000333.1:p.Glu480=
ENST00000262418.10:c.1438G= ENSP00000262418.6:p.Glu480=
ENST00000399246.3:c.777+1724G= ENSP00000382190.3:n.777+1724G=
ENST00000497360.5:n.1577G=
XM_005257593.3:c.1243G= XP_005257650.1:p.Glu415=
XM_005257593.5:c.1243G= XP_005257650.1:p.Glu415=
XM_011525129.1:c.1438G= XP_011523431.1:p.Glu480=
XM_011525129.2:c.1438G= XP_011523431.1:p.Glu480=
XM_011525130.1:c.1438G= XP_011523432.1:p.Glu480=
XM_011525131.1:c.1438G= XP_011523433.1:p.Glu480=