Canonical Allele Identifier: CA1589764842
Gene: SPINK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147831572C= , CM000667.2:g.147831572C= GRCh38
NC_000005.9:g.147211135C= , CM000667.1:g.147211135C= GRCh37
NC_000005.8:g.147191328C= NCBI36
NG_008356.2:g.12660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.6G= MANE Select ENSP00000296695.5:p.Lys2=
ENST00000296695.9:c.6G= ENSP00000296695.5:p.Lys2=
ENST00000510027.2:c.6G= ENSP00000427376.1:p.Lys2=
NM_003122.4:c.6G= NP_003113.2:p.Lys2=
NM_001354966.1:c.6G= NP_001341895.1:p.Lys2=
NM_001354966.2:c.6G= NP_001341895.1:p.Lys2=
NM_001379610.1:c.6G= MANE Select NP_001366539.1:p.Lys2=
NM_003122.5:c.6G= NP_003113.2:p.Lys2=