Canonical Allele Identifier: CA346686679
Community Standard Title: NM_000341.4(SLC3A1):c.430+2T>G
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44275967T>G , CM000664.2:g.44275967T>G GRCh38
NC_000002.11:g.44503106T>G , CM000664.1:g.44503106T>G GRCh37
NC_000002.10:g.44356610T>G NCBI36
NG_008233.1:g.5510T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.430+2T>G MANE Select NP_000332.2:n.430+2T>G
ENST00000260649.11:c.430+2T>G MANE Select ENSP00000260649.6:n.430+2T>G
NM_000341.3:c.430+2T>G NP_000332.2:n.430+2T>G
ENST00000260649.10:c.430+2T>G ENSP00000260649.6:n.430+2T>G
ENST00000409229.7:c.430+2T>G ENSP00000386620.3:n.430+2T>G
ENST00000409387.5:c.430+2T>G ENSP00000387308.1:n.430+2T>G
ENST00000409741.5:c.430+2T>G ENSP00000386954.1:n.430+2T>G
ENST00000410056.7:c.430+2T>G ENSP00000387337.3:n.430+2T>G
ENST00000611973.4:c.430+2T>G ENSP00000483618.1:n.430+2T>G
ENST00000649044.1:c.*441+2T>G ENSP00000497083.1:n.*441+2T>G
XM_011533047.1:c.430+2T>G XP_011531349.1:n.430+2T>G
XM_011533047.3:c.430+2T>G XP_011531349.1:n.430+2T>G