Canonical Allele Identifier: CA346686329
Community Standard Title: NM_000341.4(SLC3A1):c.266T>C (p.Leu89Pro)
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44275801T>C , CM000664.2:g.44275801T>C GRCh38
NC_000002.11:g.44502940T>C , CM000664.1:g.44502940T>C GRCh37
NC_000002.10:g.44356444T>C NCBI36
NG_008233.1:g.5344T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.266T>C MANE Select NP_000332.2:p.Leu89Pro
ENST00000260649.11:c.266T>C MANE Select ENSP00000260649.6:p.Leu89Pro
NM_000341.3:c.266T>C NP_000332.2:p.Leu89Pro
ENST00000260649.10:c.266T>C ENSP00000260649.6:p.Leu89Pro
ENST00000409229.7:c.266T>C ENSP00000386620.3:p.Leu89Pro
ENST00000409387.5:c.266T>C ENSP00000387308.1:p.Leu89Pro
ENST00000409741.5:c.266T>C ENSP00000386954.1:p.Leu89Pro
ENST00000410056.7:c.266T>C ENSP00000387337.3:p.Leu89Pro
ENST00000611973.4:c.266T>C ENSP00000483618.1:p.Leu89Pro
ENST00000649044.1:c.*277T>C ENSP00000497083.1:n.*277T>C
XM_011533047.1:c.266T>C XP_011531349.1:p.Leu89Pro
XM_011533047.3:c.266T>C XP_011531349.1:p.Leu89Pro