Canonical Allele Identifier: CA1589764444
Gene: SPINK1 HGNC NCBI

Linked Data

dbSNP Id: rs1756492136

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147830641G>A , CM000667.2:g.147830641G>A GRCh38
NC_000005.9:g.147210204G>A , CM000667.1:g.147210204G>A GRCh37
NC_000005.8:g.147190397G>A NCBI36
NG_008356.2:g.13591C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.55+882C>T MANE Select ENSP00000296695.5:n.55+882C>T
ENST00000296695.9:c.55+882C>T ENSP00000296695.5:n.55+882C>T
ENST00000510027.2:c.55+882C>T ENSP00000427376.1:n.55+882C>T
NM_003122.4:c.55+882C>T NP_003113.2:n.55+882C>T
NM_001354966.1:c.55+882C>T NP_001341895.1:n.55+882C>T
NM_001354966.2:c.55+882C>T NP_001341895.1:n.55+882C>T
NM_001379610.1:c.55+882C>T MANE Select NP_001366539.1:n.55+882C>T
NM_003122.5:c.55+882C>T NP_003113.2:n.55+882C>T