Canonical Allele Identifier: CA1829359287
Community Standard Title: NM_004170.6(SLC1A1):c.92-16815C=
Gene: SLC1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4527752C= , CM000671.2:g.4527752C= GRCh38
NC_000009.11:g.4527752C= , CM000671.1:g.4527752C= GRCh37
NC_000009.10:g.4517752C= NCBI36
NG_017044.1:g.42326C=

Transcript Alleles

HGVS Amino-acid Change
NM_004170.6:c.92-16815C= MANE Select NP_004161.4:n.92-16815C=
ENST00000262352.8:c.92-16815C= MANE Select ENSP00000262352.3:n.92-16815C=
NM_004170.5:c.92-16815C= NP_004161.4:n.92-16815C=
ENST00000262352.7:c.92-16815C= ENSP00000262352.3:n.92-16815C=
XM_011518007.1:c.160+7856C= XP_011516309.1:n.160+7856C=
XM_011518008.1:c.100+7856C= XP_011516310.1:n.100+7856C=
XM_011518008.3:c.100+7856C= XP_011516310.1:n.100+7856C=
XM_011518009.1:c.31+10114C= XP_011516311.1:n.31+10114C=
XM_011518009.3:c.31+10114C= XP_011516311.1:n.31+10114C=
XM_011518010.1:c.92-33697C= XP_011516312.1:n.92-33697C=
XM_017015042.1:c.160+7856C= XP_016870531.1:n.160+7856C=
XM_017015043.1:c.92-16815C= XP_016870532.1:n.92-16815C=