Canonical Allele Identifier: CA2175373536
Gene: SLC24A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134229G= , CM000677.2:g.48134229G= GRCh38
NC_000015.9:g.48426426G= , CM000677.1:g.48426426G= GRCh37
NC_000015.8:g.46213718G= NCBI36
NG_011500.1:g.18258G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.302-29G= MANE Select ENSP00000341550.3:n.302-29G=
ENST00000341459.7:c.302-29G= ENSP00000341550.3:n.302-29G=
ENST00000449382.2:c.122-29G= ENSP00000389966.2:n.122-29G=
ENST00000463289.1:n.62-29G=
NM_205850.2:c.302-29G= NP_995322.1:n.302-29G=
XM_011521458.1:c.302-29G= XP_011519760.1:n.302-29G=
XM_017022079.1:c.-38-29G= XP_016877568.1:n.-38-29G=
XM_017022080.1:c.-38-29G= XP_016877569.1:n.-38-29G=
XM_024449901.1:c.-38-29G= XP_024305669.1:n.-38-29G=
NM_205850.3:c.302-29G= MANE Select NP_995322.1:n.302-29G=