Canonical Allele Identifier: CA2671071055
Gene: SCARB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76179390del , CM000666.2:g.76179390del GRCh38
NC_000004.11:g.77100543del , CM000666.1:g.77100543del GRCh37
NC_000004.10:g.77319567del NCBI36
NG_012054.1:g.39497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682785.1:n.588+131del
ENST00000264896.8:c.612+131del MANE Select ENSP00000264896.2:n.612+131del
ENST00000502908.2:n.2244del
ENST00000638295.1:c.138+131del ENSP00000492288.1:n.138+131del
ENST00000638372.1:n.864+131del
ENST00000638603.1:c.612+131del ENSP00000491728.1:n.612+131del
ENST00000638663.1:c.612+131del ENSP00000491407.1:n.612+131del
ENST00000638680.1:n.2193+131del
ENST00000639145.1:c.603+131del ENSP00000492831.1:n.603+131del
ENST00000639300.1:c.612+131del ENSP00000492840.1:n.612+131del
ENST00000639324.1:n.711+131del
ENST00000639715.1:c.567+131del
ENST00000639738.1:c.276-13085del ENSP00000491792.1:n.276-13085del
ENST00000640076.1:n.193+131del
ENST00000640341.1:c.*252+131del ENSP00000492714.1:n.*252+131del
ENST00000640634.1:c.733+131del
ENST00000640640.1:c.612+131del ENSP00000492246.1:n.612+131del
ENST00000640916.1:n.671del
ENST00000640957.1:c.612+131del ENSP00000492004.1:n.612+131del
ENST00000264896.6:c.612+131del ENSP00000264896.2:n.612+131del
ENST00000452464.6:c.276-3476del ENSP00000399154.2:n.276-3476del
NM_001204255.1:c.276-3476del NP_001191184.1:n.276-3476del
NM_005506.3:c.612+131del NP_005497.1:n.612+131del
NM_005506.4:c.612+131del MANE Select NP_005497.1:n.612+131del
NM_001204255.2:c.276-3476del NP_001191184.1:n.276-3476del