Canonical Allele Identifier: CA1345404643
Community Standard Title: NM_014229.3(SLC6A11):c.624-8288C=
Gene: SLC6A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10835926C= , CM000665.2:g.10835926C= GRCh38
NC_000003.11:g.10877611C= , CM000665.1:g.10877611C= GRCh37
NC_000003.10:g.10852611C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014229.3:c.624-8288C= MANE Select NP_055044.1:n.624-8288C=
ENST00000254488.7:c.624-8288C= MANE Select ENSP00000254488.2:n.624-8288C=
NM_014229.1:c.624-8288C= NP_055044.1:n.624-8288C=
NM_014229.2:c.624-8288C= NP_055044.1:n.624-8288C=
ENST00000254488.6:c.624-8288C= ENSP00000254488.2:n.624-8288C=
XM_011534032.1:c.624-8288C= XP_011532334.1:n.624-8288C=
XM_011534033.1:c.624-8288C= XP_011532335.1:n.624-8288C=
XM_011534033.2:c.624-8288C= XP_011532335.1:n.624-8288C=
XM_017007073.1:c.47-5013C= XP_016862562.1:n.47-5013C=