Canonical Allele Identifier: CA8600575
Community Standard Title: NM_000342.4(SLC4A1):c.486-10C>T
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44259942G>A , CM000679.2:g.44259942G>A GRCh38
NC_000017.10:g.42337310G>A , CM000679.1:g.42337310G>A GRCh37
NC_000017.9:g.39692836G>A NCBI36
NG_007498.1:g.13193C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.486-10C>T MANE Select NP_000333.1:n.486-10C>T
ENST00000262418.12:c.486-10C>T MANE Select ENSP00000262418.6:n.486-10C>T
NM_000342.3:c.486-10C>T NP_000333.1:n.486-10C>T
ENST00000262418.10:c.486-10C>T ENSP00000262418.6:n.486-10C>T
ENST00000399246.3:c.486-10C>T ENSP00000382190.3:n.486-10C>T
ENST00000497360.5:n.625-10C>T
XM_005257593.3:c.291-10C>T XP_005257650.1:n.291-10C>T
XM_005257593.5:c.291-10C>T XP_005257650.1:n.291-10C>T
XM_011525129.1:c.486-10C>T XP_011523431.1:n.486-10C>T
XM_011525129.2:c.486-10C>T XP_011523431.1:n.486-10C>T
XM_011525130.1:c.486-10C>T XP_011523432.1:n.486-10C>T
XM_011525131.1:c.486-10C>T XP_011523433.1:n.486-10C>T