Canonical Allele Identifier: CA2175373483
Gene: SLC24A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134197T= , CM000677.2:g.48134197T= GRCh38
NC_000015.9:g.48426394T= , CM000677.1:g.48426394T= GRCh37
NC_000015.8:g.46213686T= NCBI36
NG_011500.1:g.18226T=

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.302-61T= MANE Select ENSP00000341550.3:n.302-61T=
ENST00000341459.7:c.302-61T= ENSP00000341550.3:n.302-61T=
ENST00000449382.2:c.122-61T= ENSP00000389966.2:n.122-61T=
ENST00000463289.1:n.62-61T=
NM_205850.2:c.302-61T= NP_995322.1:n.302-61T=
XM_011521458.1:c.302-61T= XP_011519760.1:n.302-61T=
XM_017022079.1:c.-38-61T= XP_016877568.1:n.-38-61T=
XM_017022080.1:c.-38-61T= XP_016877569.1:n.-38-61T=
XM_024449901.1:c.-38-61T= XP_024305669.1:n.-38-61T=
NM_205850.3:c.302-61T= MANE Select NP_995322.1:n.302-61T=