Canonical Allele Identifier: CA46490957
Community Standard Title: NM_000341.4(SLC3A1):c.638C>G (p.Pro213Arg)
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44281414C>G , CM000664.2:g.44281414C>G GRCh38
NC_000002.11:g.44508553C>G , CM000664.1:g.44508553C>G GRCh37
NC_000002.10:g.44362057C>G NCBI36
NG_008233.1:g.10957C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.638C>G MANE Select NP_000332.2:p.Pro213Arg
ENST00000260649.11:c.638C>G MANE Select ENSP00000260649.6:p.Pro213Arg
NM_000341.3:c.638C>G NP_000332.2:p.Pro213Arg
ENST00000260649.10:c.638C>G ENSP00000260649.6:p.Pro213Arg
ENST00000409229.7:c.638C>G ENSP00000386620.3:p.Pro213Arg
ENST00000409387.5:c.638C>G ENSP00000387308.1:p.Pro213Arg
ENST00000409741.5:c.638C>G ENSP00000386954.1:p.Pro213Arg
ENST00000410056.7:c.638C>G ENSP00000387337.3:p.Pro213Arg
ENST00000611973.4:c.638C>G ENSP00000483618.1:p.Pro213Arg
ENST00000649044.1:c.*649C>G ENSP00000497083.1:n.*649C>G
XM_011533047.1:c.638C>G XP_011531349.1:p.Pro213Arg
XM_011533047.3:c.638C>G XP_011531349.1:p.Pro213Arg