Canonical Allele Identifier: CA8600221
Community Standard Title: NM_000342.4(SLC4A1):c.1671G>A (p.Val557=)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44255802C>T , CM000679.2:g.44255802C>T GRCh38
NC_000017.10:g.42333170C>T , CM000679.1:g.42333170C>T GRCh37
NC_000017.9:g.39688696C>T NCBI36
NG_007498.1:g.17333G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.1671G>A MANE Select NP_000333.1:p.Val557=
ENST00000262418.12:c.1671G>A MANE Select ENSP00000262418.6:p.Val557=
NM_000342.3:c.1671G>A NP_000333.1:p.Val557=
ENST00000262418.10:c.1671G>A ENSP00000262418.6:p.Val557=
ENST00000399246.3:c.778-581G>A ENSP00000382190.3:n.778-581G>A
XM_005257593.3:c.1476G>A XP_005257650.1:p.Val492=
XM_005257593.5:c.1476G>A XP_005257650.1:p.Val492=
XM_011525129.1:c.1671G>A XP_011523431.1:p.Val557=
XM_011525129.2:c.1671G>A XP_011523431.1:p.Val557=
XM_011525130.1:c.1671G>A XP_011523432.1:p.Val557=
XM_011525131.1:c.1671G>A XP_011523433.1:p.Val557=