Canonical Allele Identifier: CA35752081
Gene: KISS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1258690
ClinVar RCV Id: RCV001671220
dbSNP Id: rs200451423
gnomAD v2: 1-204159537-T-TTG
gnomAD v3: 1-204190409-T-TTG
gnomAD v4: 1-204190409-T-TTG
MyVariant Identifiers: chr1:g.204159537_204159538insTG (hg19) chr1:g.204159538_204159540delinsTGCCC (hg19) chr1:g.204190409_204190410insTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190409_204190410insTG , CM000663.2:g.204190409_204190410insTG GRCh38
NC_000001.10:g.204159537_204159538insTG , CM000663.1:g.204159537_204159538insTG GRCh37
NC_000001.9:g.202426160_202426161insTG NCBI36
NG_032151.1:g.11082_11083insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367194.5:c.*74_*75insCA MANE Select ENSP00000356162.4:n.*74_*75insCA
ENST00000367194.4:c.*74_*75insCA ENSP00000356162.4:n.*74_*75insCA
NM_002256.3:c.*74_*75insCA NP_002247.3:n.*74_*75insCA
XM_011509525.1:c.*74_*75insCA XP_011507827.1:n.*74_*75insCA
NM_002256.4:c.*74_*75insCA MANE Select NP_002247.3:n.*74_*75insCA
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