Canonical Allele Identifier: CA8600097
Community Standard Title: NM_000342.4(SLC4A1):c.2193C>T (p.Ser731=)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44253236G>A , CM000679.2:g.44253236G>A GRCh38
NC_000017.10:g.42330604G>A , CM000679.1:g.42330604G>A GRCh37
NC_000017.9:g.39686130G>A NCBI36
NG_007498.1:g.19899C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.2193C>T MANE Select NP_000333.1:p.Ser731=
ENST00000262418.12:c.2193C>T MANE Select ENSP00000262418.6:p.Ser731=
NM_000342.3:c.2193C>T NP_000333.1:p.Ser731=
ENST00000262418.10:c.2193C>T ENSP00000262418.6:p.Ser731=
ENST00000399246.3:c.1095C>T ENSP00000382190.3:p.Ser365=
XM_005257593.3:c.1998C>T XP_005257650.1:p.Ser666=
XM_005257593.5:c.1998C>T XP_005257650.1:p.Ser666=
XM_011525129.1:c.2103C>T XP_011523431.1:p.Ser701=
XM_011525129.2:c.2103C>T XP_011523431.1:p.Ser701=
XM_011525130.1:c.2193C>T XP_011523432.1:p.Ser731=