Canonical Allele Identifier: CA3587543

Gene: PROP1

Linked Data

• dbSNP Id: rs749055035
• ExAC: 5:177420090 T / G
• gnomAD v2: 5-177420090-T-G
• gnomAD v4: 5-177993089-T-G
• MyVariant Identifiers: chr5:g.177420090T>G (hg19) ; chr5:g.177993089T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177993089T>G , CM000667.2:g.177993089T>G	GRCh38
NC_000005.9:g.177420090T>G , CM000667.1:g.177420090T>G	GRCh37
NC_000005.8:g.177352696T>G	NCBI36
NG_015889.1:g.8154A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.343-42A>C MANE Select	ENSP00000311290.2:n.343-42A>C
NM_006261.4:c.343-42A>C	NP_006252.3:n.343-42A>C
NM_006261.5:c.343-42A>C MANE Select	NP_006252.4:n.343-42A>C