Canonical Allele Identifier: CA10621447
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 353021
ClinVar RCV Id: RCV000297903 RCV001537295
dbSNP Id: rs150629697
gnomAD v2: 5-177423236-C-T
gnomAD v3: 5-177996235-C-T
gnomAD v4: 5-177996235-C-T
MyVariant Identifiers: chr5:g.177423236C>T (hg19) chr5:g.177996235C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177996235C>T , CM000667.2:g.177996235C>T GRCh38
NC_000005.9:g.177423236C>T , CM000667.1:g.177423236C>T GRCh37
NC_000005.8:g.177355842C>T NCBI36
NG_015889.1:g.5008G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.-302G>A MANE Select ENSP00000311290.2:n.-302G>A
NM_006261.4:c.-302G>A NP_006252.3:n.-302G>A
NM_006261.5:c.-302G>A MANE Select NP_006252.4:n.-302G>A
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