Canonical Allele Identifier: CA2580610964
Community Standard Title: NM_005629.4(SLC6A8):c.1495+5G>C
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694451G>C , CM000685.2:g.153694451G>C GRCh38
NC_000023.10:g.152959906G>C , CM000685.1:g.152959906G>C GRCh37
NC_000023.9:g.152613100G>C NCBI36
NG_012016.1:g.11155G>C
NG_012016.2:g.11155G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005629.4:c.1495+5G>C MANE Select NP_005620.1:n.1495+5G>C
ENST00000253122.10:c.1495+5G>C MANE Select ENSP00000253122.5:n.1495+5G>C
NM_001142805.1:c.1465+5G>C NP_001136277.1:n.1465+5G>C
NM_001142805.2:c.1465+5G>C NP_001136277.1:n.1465+5G>C
NM_001142806.1:c.1150+5G>C NP_001136278.1:n.1150+5G>C
NM_005629.3:c.1495+5G>C NP_005620.1:n.1495+5G>C
ENST00000253122.9:c.1495+5G>C ENSP00000253122.5:n.1495+5G>C
ENST00000413787.1:c.424+5G>C ENSP00000400463.1:n.424+5G>C
ENST00000430077.6:c.1150+5G>C ENSP00000403041.2:n.1150+5G>C
ENST00000485324.1:n.1721G>C