Canonical Allele Identifier: CA99838746

Gene: SCARB2

Linked Data

• dbSNP Id: rs951660672
• MyVariant Identifiers: chr4:g.77100443_77100444insG (hg19) ; chr4:g.76179290_76179291insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179290_76179291insG , CM000666.2:g.76179290_76179291insG	GRCh38
NC_000004.11:g.77100443_77100444insG , CM000666.1:g.77100443_77100444insG	GRCh37
NC_000004.10:g.77319467_77319468insG	NCBI36
NG_012054.1:g.39592_39593insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.588+226_588+227insC
ENST00000264896.8:c.612+226_612+227insC MANE Select	ENSP00000264896.2:n.612+226_612+227insC
ENST00000502908.2:n.2339_2340insC
ENST00000638295.1:c.138+226_138+227insC	ENSP00000492288.1:n.138+226_138+227insC
ENST00000638372.1:n.864+226_864+227insC
ENST00000638603.1:c.612+226_612+227insC	ENSP00000491728.1:n.612+226_612+227insC
ENST00000638663.1:c.612+226_612+227insC	ENSP00000491407.1:n.612+226_612+227insC
ENST00000638680.1:n.2193+226_2193+227insC
ENST00000639145.1:c.603+226_603+227insC	ENSP00000492831.1:n.603+226_603+227insC
ENST00000639300.1:c.612+226_612+227insC	ENSP00000492840.1:n.612+226_612+227insC
ENST00000639324.1:n.711+226_711+227insC
ENST00000639715.1:c.567+226_567+227insC
ENST00000639738.1:c.276-12990_276-12989insC	ENSP00000491792.1:n.276-12990_276-12989insC
ENST00000640076.1:n.193+226_193+227insC
ENST00000640341.1:c.*252+226_*252+227insC	ENSP00000492714.1:n.*252+226_*252+227insC
ENST00000640634.1:c.733+226_733+227insC
ENST00000640640.1:c.612+226_612+227insC	ENSP00000492246.1:n.612+226_612+227insC
ENST00000640957.1:c.612+226_612+227insC	ENSP00000492004.1:n.612+226_612+227insC
ENST00000264896.6:c.612+226_612+227insC	ENSP00000264896.2:n.612+226_612+227insC
ENST00000452464.6:c.276-3381_276-3380insC	ENSP00000399154.2:n.276-3381_276-3380insC
NM_001204255.1:c.276-3381_276-3380insC	NP_001191184.1:n.276-3381_276-3380insC
NM_005506.3:c.612+226_612+227insC	NP_005497.1:n.612+226_612+227insC
NM_005506.4:c.612+226_612+227insC MANE Select	NP_005497.1:n.612+226_612+227insC
NM_001204255.2:c.276-3381_276-3380insC	NP_001191184.1:n.276-3381_276-3380insC