Canonical Allele Identifier: CA46490820
Community Standard Title: NM_000341.4(SLC3A1):c.611-212dup
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44281175dup , CM000664.2:g.44281175dup GRCh38
NC_000002.11:g.44508314dup , CM000664.1:g.44508314dup GRCh37
NC_000002.10:g.44361818dup NCBI36
NG_008233.1:g.10718dup

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.611-212dup MANE Select NP_000332.2:n.611-212dup
ENST00000260649.11:c.611-212dup MANE Select ENSP00000260649.6:n.611-212dup
NM_000341.3:c.611-212dup NP_000332.2:n.611-212dup
ENST00000260649.10:c.611-212dup ENSP00000260649.6:n.611-212dup
ENST00000409229.7:c.611-212dup ENSP00000386620.3:n.611-212dup
ENST00000409387.5:c.611-212dup ENSP00000387308.1:n.611-212dup
ENST00000409741.5:c.611-212dup ENSP00000386954.1:n.611-212dup
ENST00000410056.7:c.611-212dup ENSP00000387337.3:n.611-212dup
ENST00000611973.4:c.611-212dup ENSP00000483618.1:n.611-212dup
ENST00000649044.1:c.*622-212dup ENSP00000497083.1:n.*622-212dup
XM_011533047.1:c.611-212dup XP_011531349.1:n.611-212dup
XM_011533047.3:c.611-212dup XP_011531349.1:n.611-212dup