Canonical Allele Identifier: CA1589764429
Gene: SPINK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147830605T= , CM000667.2:g.147830605T= GRCh38
NC_000005.9:g.147210168T= , CM000667.1:g.147210168T= GRCh37
NC_000005.8:g.147190361T= NCBI36
NG_008356.2:g.13627A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.55+918A= MANE Select ENSP00000296695.5:n.55+918A=
ENST00000296695.9:c.55+918A= ENSP00000296695.5:n.55+918A=
ENST00000510027.2:c.55+918A= ENSP00000427376.1:n.55+918A=
NM_003122.4:c.55+918A= NP_003113.2:n.55+918A=
NM_001354966.1:c.55+918A= NP_001341895.1:n.55+918A=
NM_001354966.2:c.55+918A= NP_001341895.1:n.55+918A=
NM_001379610.1:c.55+918A= MANE Select NP_001366539.1:n.55+918A=
NM_003122.5:c.55+918A= NP_003113.2:n.55+918A=