Canonical Allele Identifier: CA1640202
Community Standard Title: NM_000341.4(SLC3A1):c.647C>T (p.Thr216Met)
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44281423C>T , CM000664.2:g.44281423C>T GRCh38
NC_000002.11:g.44508562C>T , CM000664.1:g.44508562C>T GRCh37
NC_000002.10:g.44362066C>T NCBI36
NG_008233.1:g.10966C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.647C>T MANE Select NP_000332.2:p.Thr216Met
ENST00000260649.11:c.647C>T MANE Select ENSP00000260649.6:p.Thr216Met
NM_000341.3:c.647C>T NP_000332.2:p.Thr216Met
ENST00000260649.10:c.647C>T ENSP00000260649.6:p.Thr216Met
ENST00000409229.7:c.647C>T ENSP00000386620.3:p.Thr216Met
ENST00000409387.5:c.647C>T ENSP00000387308.1:p.Thr216Met
ENST00000409741.5:c.647C>T ENSP00000386954.1:p.Thr216Met
ENST00000410056.7:c.647C>T ENSP00000387337.3:p.Thr216Met
ENST00000611973.4:c.647C>T ENSP00000483618.1:p.Thr216Met
ENST00000649044.1:c.*658C>T ENSP00000497083.1:n.*658C>T
XM_011533047.1:c.647C>T XP_011531349.1:p.Thr216Met
XM_011533047.3:c.647C>T XP_011531349.1:p.Thr216Met