Canonical Allele Identifier: CA344346887
Gene: KISS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2617687
ClinVar RCV Id: RCV004359443
dbSNP Id: rs1194935052
gnomAD v2: 1-204159874-G-C
gnomAD v3: 1-204190746-G-C
gnomAD v4: 1-204190746-G-C
MyVariant Identifiers: chr1:g.204159874G>C (hg19) chr1:g.204190746G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190746G>C , CM000663.2:g.204190746G>C GRCh38
NC_000001.10:g.204159874G>C , CM000663.1:g.204159874G>C GRCh37
NC_000001.9:g.202426497G>C NCBI36
NG_032151.1:g.10746C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367194.5:c.155C>G MANE Select ENSP00000356162.4:p.Pro52Arg
ENST00000367194.4:c.155C>G ENSP00000356162.4:p.Pro52Arg
ENST00000625357.1:c.155C>G ENSP00000485957.1:p.Pro52Arg
NM_002256.3:c.155C>G NP_002247.3:p.Pro52Arg
XM_011509525.1:c.155C>G XP_011507827.1:p.Pro52Arg
NM_002256.4:c.155C>G MANE Select NP_002247.3:p.Pro52Arg
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