Canonical Allele Identifier: CA915952641
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 654583
ClinVar RCV Id: RCV000810578
dbSNP Id: rs1601803431

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.36936861dup , CM000683.2:g.36936861dup GRCh38
NC_000021.8:g.38309161dup , CM000683.1:g.38309161dup GRCh37
NC_000021.7:g.37231031dup NCBI36
NG_016193.1:g.58376dup
NG_016193.2:g.58534dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000674895.3:c.1025dup MANE Select ENSP00000502087.2:p.Tyr342Ter
ENST00000674895.2:c.584dup ENSP00000502087.1:p.Tyr195Ter
ENST00000675057.1:c.584dup ENSP00000501832.1:p.Tyr195Ter
ENST00000675307.1:c.584dup ENSP00000501750.1:p.Tyr195Ter
ENST00000336648.8:c.584dup ENSP00000338387.3:p.Tyr195Ter
ENST00000399120.5:c.584dup ENSP00000382071.1:p.Tyr195Ter
ENST00000612277.4:c.584dup ENSP00000479939.1:p.Tyr195Ter
NM_000411.6:c.584dup NP_000402.3:p.Tyr195Ter
NM_001242784.1:c.584dup NP_001229713.1:p.Tyr195Ter
NM_001242785.1:c.584dup NP_001229714.1:p.Tyr195Ter
XM_005260953.2:c.1025dup XP_005261010.1:p.Tyr342Ter
XM_005260954.1:c.1025dup XP_005261011.1:p.Tyr342Ter
XM_005260955.2:c.584dup XP_005261012.1:p.Tyr195Ter
XM_005260956.2:c.584dup XP_005261013.1:p.Tyr195Ter
XM_006723994.1:c.584dup XP_006724057.1:p.Tyr195Ter
XM_006723995.1:c.584dup XP_006724058.1:p.Tyr195Ter
XM_011529538.1:c.584dup XP_011527840.1:p.Tyr195Ter
XM_011529539.1:c.584dup XP_011527841.1:p.Tyr195Ter
XM_011529540.1:c.1025dup XP_011527842.1:p.Tyr342Ter
XM_011529541.1:c.584dup XP_011527843.1:p.Tyr195Ter
XM_011529542.1:c.1025dup XP_011527844.1:p.Tyr342Ter
NM_000411.7:c.584dup NP_000402.3:p.Tyr195Ter
NM_001242784.2:c.584dup NP_001229713.1:p.Tyr195Ter
NM_001242785.2:c.584dup NP_001229714.1:p.Tyr195Ter
NM_001352514.1:c.1025dup NP_001339443.1:p.Tyr342Ter
NM_001352515.1:c.584dup NP_001339444.1:p.Tyr195Ter
NM_001352516.1:c.584dup NP_001339445.1:p.Tyr195Ter
NM_001352517.1:c.584dup NP_001339446.1:p.Tyr195Ter
NM_001352518.1:c.584dup NP_001339447.1:p.Tyr195Ter
NR_148020.1:n.1067dup
NR_148021.1:n.1041dup
XM_011529539.3:c.584dup XP_011527841.1:p.Tyr195Ter
XM_011529540.2:c.1025dup XP_011527842.1:p.Tyr342Ter
XM_017028330.1:c.584dup XP_016883819.1:p.Tyr195Ter
XM_024452065.1:c.413dup XP_024307833.1:p.Tyr138Ter
XM_024452066.1:c.413dup XP_024307834.1:p.Tyr138Ter
XR_001754835.1:n.1026dup
XR_001754836.1:n.1026dup
XR_001754837.2:n.1026dup
XR_001754840.1:n.1026dup
NM_000411.8:c.584dup NP_000402.3:p.Tyr195Ter
NM_001242784.3:c.584dup NP_001229713.1:p.Tyr195Ter
NM_001352514.2:c.1025dup MANE Select NP_001339443.1:p.Tyr342Ter
NM_001352515.2:c.584dup NP_001339444.1:p.Tyr195Ter
NM_001352516.2:c.584dup NP_001339445.1:p.Tyr195Ter
NR_148020.2:n.884dup
NM_001352518.2:c.584dup NP_001339447.1:p.Tyr195Ter