Canonical Allele Identifier: CA2676774020
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992574-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992574T>G , CM000667.2:g.177992574T>G GRCh38
NC_000005.9:g.177419575T>G , CM000667.1:g.177419575T>G GRCh37
NC_000005.8:g.177352181T>G NCBI36
NG_015889.1:g.8669A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*135A>C MANE Select ENSP00000311290.2:n.*135A>C
NM_006261.4:c.*135A>C NP_006252.3:n.*135A>C
NM_006261.5:c.*135A>C MANE Select NP_006252.4:n.*135A>C
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