Canonical Allele Identifier: CA10653610
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 339948
ClinVar RCV Id: RCV000376523
dbSNP Id: rs886057071

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.36753261G>T , CM000683.2:g.36753261G>T GRCh38
NC_000021.8:g.38125562G>T , CM000683.1:g.38125562G>T GRCh37
NC_000021.7:g.37047432G>T NCBI36
NG_016193.1:g.241975C>A
NG_016193.2:g.242134C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000674895.3:c.*985C>A MANE Select ENSP00000502087.2:n.*985C>A
ENST00000674895.2:c.*985C>A ENSP00000502087.1:n.*985C>A
ENST00000675057.1:c.*1576C>A ENSP00000501832.1:n.*1576C>A
ENST00000675307.1:c.*985C>A ENSP00000501750.1:n.*985C>A
ENST00000336648.8:c.*985C>A ENSP00000338387.3:n.*985C>A
ENST00000399120.5:c.*985C>A ENSP00000382071.1:n.*985C>A
ENST00000612277.4:c.*985C>A ENSP00000479939.1:n.*985C>A
NM_000411.6:c.*985C>A NP_000402.3:n.*985C>A
NM_001242784.1:c.*985C>A NP_001229713.1:n.*985C>A
NM_001242785.1:c.*985C>A NP_001229714.1:n.*985C>A
XM_005260953.2:c.*985C>A XP_005261010.1:n.*985C>A
XM_005260955.2:c.*985C>A XP_005261012.1:n.*985C>A
XM_005260956.2:c.*985C>A XP_005261013.1:n.*985C>A
XM_006723994.1:c.*985C>A XP_006724057.1:n.*985C>A
XM_006723995.1:c.*985C>A XP_006724058.1:n.*985C>A
XM_011529538.1:c.*985C>A XP_011527840.1:n.*985C>A
XM_011529539.1:c.*985C>A XP_011527841.1:n.*985C>A
XM_011529541.1:c.*985C>A XP_011527843.1:n.*985C>A
NM_000411.7:c.*985C>A NP_000402.3:n.*985C>A
NM_001242784.2:c.*985C>A NP_001229713.1:n.*985C>A
NM_001242785.2:c.*985C>A NP_001229714.1:n.*985C>A
NM_001352514.1:c.*985C>A NP_001339443.1:n.*985C>A
NM_001352515.1:c.*985C>A NP_001339444.1:n.*985C>A
NM_001352516.1:c.*985C>A NP_001339445.1:n.*985C>A
NM_001352517.1:c.*985C>A NP_001339446.1:n.*985C>A
NM_001352518.1:c.*985C>A NP_001339447.1:n.*985C>A
NR_148020.1:n.3874C>A
NR_148021.1:n.3848C>A
XM_011529539.3:c.*985C>A XP_011527841.1:n.*985C>A
XM_017028330.1:c.*985C>A XP_016883819.1:n.*985C>A
XM_024452065.1:c.*985C>A XP_024307833.1:n.*985C>A
XM_024452066.1:c.*985C>A XP_024307834.1:n.*985C>A
XR_001754835.1:n.3833C>A
XR_001754836.1:n.3447C>A
NM_000411.8:c.*985C>A NP_000402.3:n.*985C>A
NM_001242784.3:c.*985C>A NP_001229713.1:n.*985C>A
NM_001352514.2:c.*985C>A MANE Select NP_001339443.1:n.*985C>A
NM_001352515.2:c.*985C>A NP_001339444.1:n.*985C>A
NM_001352516.2:c.*985C>A NP_001339445.1:n.*985C>A
NR_148020.2:n.3691C>A
NM_001352518.2:c.*985C>A NP_001339447.1:n.*985C>A