Canonical Allele Identifier: CA2175373559
Gene: SLC24A5 HGNC NCBI

Linked Data

dbSNP Id: rs2038840175

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134241_48134242insAA , CM000677.2:g.48134241_48134242insAA GRCh38
NC_000015.9:g.48426438_48426439insAA , CM000677.1:g.48426438_48426439insAA GRCh37
NC_000015.8:g.46213730_46213731insAA NCBI36
NG_011500.1:g.18270_18271insAA

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.302-17_302-16insAA MANE Select ENSP00000341550.3:n.302-17_302-16insAA
ENST00000341459.7:c.302-17_302-16insAA ENSP00000341550.3:n.302-17_302-16insAA
ENST00000449382.2:c.122-17_122-16insAA ENSP00000389966.2:n.122-17_122-16insAA
ENST00000463289.1:n.62-17_62-16insAA
NM_205850.2:c.302-17_302-16insAA NP_995322.1:n.302-17_302-16insAA
XM_011521458.1:c.302-17_302-16insAA XP_011519760.1:n.302-17_302-16insAA
XM_017022079.1:c.-38-17_-38-16insAA XP_016877568.1:n.-38-17_-38-16insAA
XM_017022080.1:c.-38-17_-38-16insAA XP_016877569.1:n.-38-17_-38-16insAA
XM_024449901.1:c.-38-17_-38-16insAA XP_024305669.1:n.-38-17_-38-16insAA
NM_205850.3:c.302-17_302-16insAA MANE Select NP_995322.1:n.302-17_302-16insAA