Canonical Allele Identifier: CA1956619624
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20627804C= , CM000673.2:g.20627804C= GRCh38
NC_000011.9:g.20649350C= , CM000673.1:g.20649350C= GRCh37
NC_000011.8:g.20605926C= NCBI36
NG_013086.1:g.33405C=
NG_013086.2:g.33405C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525748.6:c.1396-176C= MANE Select ENSP00000434364.2:n.1396-176C=
ENST00000298923.11:c.*693-176C= ENSP00000298923.7:n.*693-176C=
ENST00000525748.5:c.1396-176C= ENSP00000434364.1:n.1396-176C=
NM_004211.3:c.1396-176C= NP_004202.2:n.1396-176C=
XM_005253225.1:c.694-176C= XP_005253282.1:n.694-176C=
XM_011520473.1:c.1396-176C= XP_011518775.1:n.1396-176C=
NM_001318369.1:c.694-176C= NP_001305298.1:n.694-176C=
NM_004211.4:c.1396-176C= NP_004202.3:n.1396-176C=
XM_017018544.2:c.520-176C= XP_016874033.1:n.520-176C=
XM_017018545.2:c.355-176C= XP_016874034.1:n.355-176C=
NM_001318369.2:c.694-176C= NP_001305298.1:n.694-176C=
NM_004211.5:c.1396-176C= MANE Select NP_004202.4:n.1396-176C=