Canonical Allele Identifier: CA357603495
Gene: DSPP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87612592A>C , CM000666.2:g.87612592A>C GRCh38
NC_000004.11:g.88533744A>C , CM000666.1:g.88533744A>C GRCh37
NC_000004.10:g.88752768A>C NCBI36
NG_011595.1:g.9064A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651931.1:c.406A>C MANE Select ENSP00000498766.1:p.Ile136Leu
ENST00000282478.7:c.406A>C ENSP00000282478.7:p.Ile136Leu
ENST00000399271.5:c.406A>C ENSP00000382213.1:p.Ile136Leu
NM_014208.3:c.406A>C MANE Select NP_055023.2:p.Ile136Leu