Canonical Allele Identifier: CA805371970
Gene: SPINK1 HGNC NCBI

Linked Data

dbSNP Id: rs148434824
MyVariant Identifiers: chr5:g.147211155G>C (hg19) chr5:g.147831592G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147831592G>C , CM000667.2:g.147831592G>C GRCh38
NC_000005.9:g.147211155G>C , CM000667.1:g.147211155G>C GRCh37
NC_000005.8:g.147191348G>C NCBI36
NG_008356.2:g.12640C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.-15C>G MANE Select ENSP00000296695.5:n.-15C>G
ENST00000296695.9:c.-15C>G ENSP00000296695.5:n.-15C>G
ENST00000510027.2:c.-15C>G ENSP00000427376.1:n.-15C>G
NM_003122.4:c.-15C>G NP_003113.2:n.-15C>G
NM_001354966.1:c.-15C>G NP_001341895.1:n.-15C>G
NM_001354966.2:c.-15C>G NP_001341895.1:n.-15C>G
NM_001379610.1:c.-15C>G MANE Select NP_001366539.1:n.-15C>G
NM_003122.5:c.-15C>G NP_003113.2:n.-15C>G
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