Canonical Allele Identifier: CA2175373531
Gene: SLC24A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134226T= , CM000677.2:g.48134226T= GRCh38
NC_000015.9:g.48426423T= , CM000677.1:g.48426423T= GRCh37
NC_000015.8:g.46213715T= NCBI36
NG_011500.1:g.18255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341459.8:c.302-32T= MANE Select ENSP00000341550.3:n.302-32T=
ENST00000341459.7:c.302-32T= ENSP00000341550.3:n.302-32T=
ENST00000449382.2:c.122-32T= ENSP00000389966.2:n.122-32T=
ENST00000463289.1:n.62-32T=
NM_205850.2:c.302-32T= NP_995322.1:n.302-32T=
XM_011521458.1:c.302-32T= XP_011519760.1:n.302-32T=
XM_017022079.1:c.-38-32T= XP_016877568.1:n.-38-32T=
XM_017022080.1:c.-38-32T= XP_016877569.1:n.-38-32T=
XM_024449901.1:c.-38-32T= XP_024305669.1:n.-38-32T=
NM_205850.3:c.302-32T= MANE Select NP_995322.1:n.302-32T=