Canonical Allele Identifier: CA1603814042
Gene: PROP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992919G= , CM000667.2:g.177992919G= GRCh38
NC_000005.9:g.177419920G= , CM000667.1:g.177419920G= GRCh37
NC_000005.8:g.177352526G= NCBI36
NG_015889.1:g.8324C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.471C= MANE Select ENSP00000311290.2:p.Tyr157=
NM_006261.4:c.471C= NP_006252.3:p.Tyr157=
NM_006261.5:c.471C= MANE Select NP_006252.4:p.Tyr157=
Search 100 bp 5'
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