Canonical Allele Identifier: CA8600355
Community Standard Title: NM_000342.4(SLC4A1):c.1172C>T (p.Pro391Leu)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44258096G>A , CM000679.2:g.44258096G>A GRCh38
NC_000017.10:g.42335464G>A , CM000679.1:g.42335464G>A GRCh37
NC_000017.9:g.39690990G>A NCBI36
NG_007498.1:g.15039C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.1172C>T MANE Select NP_000333.1:p.Pro391Leu
ENST00000262418.12:c.1172C>T MANE Select ENSP00000262418.6:p.Pro391Leu
NM_000342.3:c.1172C>T NP_000333.1:p.Pro391Leu
ENST00000262418.10:c.1172C>T ENSP00000262418.6:p.Pro391Leu
ENST00000399246.3:c.777+1166C>T ENSP00000382190.3:n.777+1166C>T
ENST00000497360.5:n.1311C>T
XM_005257593.3:c.977C>T XP_005257650.1:p.Pro326Leu
XM_005257593.5:c.977C>T XP_005257650.1:p.Pro326Leu
XM_011525129.1:c.1172C>T XP_011523431.1:p.Pro391Leu
XM_011525129.2:c.1172C>T XP_011523431.1:p.Pro391Leu
XM_011525130.1:c.1172C>T XP_011523432.1:p.Pro391Leu
XM_011525131.1:c.1172C>T XP_011523433.1:p.Pro391Leu