Canonical Allele Identifier: CA2175373431
Gene: SLC24A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134131_48134136delinsGTATTT , CM000677.2:g.48134131_48134136delinsGTATTT GRCh38
NC_000015.9:g.48426328_48426333delinsGTATTT , CM000677.1:g.48426328_48426333delinsGTATTT GRCh37
NC_000015.8:g.46213620_46213625delinsGTATTT NCBI36
NG_011500.1:g.18160_18165delinsGTATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000341459.8:c.302-127_302-122delinsGTATTT MANE Select ENSP00000341550.3:n.302-127_302-122delinsGTATTT
ENST00000341459.7:c.302-127_302-122delinsGTATTT ENSP00000341550.3:n.302-127_302-122delinsGTATTT
ENST00000449382.2:c.122-127_122-122delinsGTATTT ENSP00000389966.2:n.122-127_122-122delinsGTATTT
ENST00000463289.1:n.62-127_62-122delinsGTATTT
NM_205850.2:c.302-127_302-122delinsGTATTT NP_995322.1:n.302-127_302-122delinsGTATTT
XM_011521458.1:c.302-127_302-122delinsGTATTT XP_011519760.1:n.302-127_302-122delinsGTATTT
XM_017022079.1:c.-38-127_-38-122delinsGTATTT XP_016877568.1:n.-38-127_-38-122delinsGTATTT
XM_017022080.1:c.-38-127_-38-122delinsGTATTT XP_016877569.1:n.-38-127_-38-122delinsGTATTT
XM_024449901.1:c.-38-127_-38-122delinsGTATTT XP_024305669.1:n.-38-127_-38-122delinsGTATTT
NM_205850.3:c.302-127_302-122delinsGTATTT MANE Select NP_995322.1:n.302-127_302-122delinsGTATTT