Canonical Allele Identifier: CA3494828
Gene: SPINK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 440295
dbSNP Id: rs147454311

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147831545G>A , CM000667.2:g.147831545G>A GRCh38
NC_000005.9:g.147211108G>A , CM000667.1:g.147211108G>A GRCh37
NC_000005.8:g.147191301G>A NCBI36
NG_008356.2:g.12687C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.33C>T MANE Select ENSP00000296695.5:p.Ala11=
ENST00000296695.9:c.33C>T ENSP00000296695.5:p.Ala11=
ENST00000510027.2:c.33C>T ENSP00000427376.1:p.Ala11=
NM_003122.4:c.33C>T NP_003113.2:p.Ala11=
NM_001354966.1:c.33C>T NP_001341895.1:p.Ala11=
NM_001354966.2:c.33C>T NP_001341895.1:p.Ala11=
NM_001379610.1:c.33C>T MANE Select NP_001366539.1:p.Ala11=
NM_003122.5:c.33C>T NP_003113.2:p.Ala11=