Canonical Allele Identifier: CA362378793

Gene: PROP1

Linked Data

• dbSNP Id: rs1772693142
• MyVariant Identifiers: chr5:g.177419985C>A (hg19) ; chr5:g.177992984C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992984C>A , CM000667.2:g.177992984C>A	GRCh38
NC_000005.9:g.177419985C>A , CM000667.1:g.177419985C>A	GRCh37
NC_000005.8:g.177352591C>A	NCBI36
NG_015889.1:g.8259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.406G>T MANE Select	ENSP00000311290.2:p.Ala136Ser
NM_006261.4:c.406G>T	NP_006252.3:p.Ala136Ser
NM_006261.5:c.406G>T MANE Select	NP_006252.4:p.Ala136Ser