Canonical Allele Identifier: CA46490735
Community Standard Title: NM_000341.4(SLC3A1):c.610+122_610+125dup
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44281017_44281020dup , CM000664.2:g.44281017_44281020dup GRCh38
NC_000002.11:g.44508156_44508159dup , CM000664.1:g.44508156_44508159dup GRCh37
NC_000002.10:g.44361660_44361663dup NCBI36
NG_008233.1:g.10560_10563dup

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.610+122_610+125dup MANE Select NP_000332.2:n.610+122_610+125dup
ENST00000260649.11:c.610+122_610+125dup MANE Select ENSP00000260649.6:n.610+122_610+125dup
NM_000341.3:c.610+122_610+125dup NP_000332.2:n.610+122_610+125dup
ENST00000260649.10:c.610+122_610+125dup ENSP00000260649.6:n.610+122_610+125dup
ENST00000409229.7:c.610+122_610+125dup ENSP00000386620.3:n.610+122_610+125dup
ENST00000409387.5:c.610+122_610+125dup ENSP00000387308.1:n.610+122_610+125dup
ENST00000409741.5:c.610+122_610+125dup ENSP00000386954.1:n.610+122_610+125dup
ENST00000410056.7:c.610+122_610+125dup ENSP00000387337.3:n.610+122_610+125dup
ENST00000611973.4:c.610+122_610+125dup ENSP00000483618.1:n.610+122_610+125dup
ENST00000649044.1:c.*621+122_*621+125dup ENSP00000497083.1:n.*621+122_*621+125dup
XM_011533047.1:c.610+122_610+125dup XP_011531349.1:n.610+122_610+125dup
XM_011533047.3:c.610+122_610+125dup XP_011531349.1:n.610+122_610+125dup