Canonical Allele Identifier: CA2255105429
Gene: SLC6A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30211722T= , CM000679.2:g.30211722T= GRCh38
NC_000017.10:g.28538740T= , CM000679.1:g.28538740T= GRCh37
NC_000017.9:g.25562866T= NCBI36
NG_011747.2:g.29215A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650711.1:c.1205-298A= MANE Select ENSP00000498537.1:n.1205-298A=
ENST00000261707.7:c.1205-298A= ENSP00000261707.3:n.1205-298A=
ENST00000394821.2:c.1205-298A= ENSP00000378298.2:n.1205-298A=
ENST00000401766.6:c.1205-298A= ENSP00000385822.2:n.1205-298A=
NM_001045.5:c.1205-298A= NP_001036.1:n.1205-298A=
NM_001045.6:c.1205-298A= MANE Select NP_001036.1:n.1205-298A=
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