Canonical Allele Identifier: CA1589764455
Gene: SPINK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147830658G= , CM000667.2:g.147830658G= GRCh38
NC_000005.9:g.147210221G= , CM000667.1:g.147210221G= GRCh37
NC_000005.8:g.147190414G= NCBI36
NG_008356.2:g.13574C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296695.10:c.55+865C= MANE Select ENSP00000296695.5:n.55+865C=
ENST00000296695.9:c.55+865C= ENSP00000296695.5:n.55+865C=
ENST00000510027.2:c.55+865C= ENSP00000427376.1:n.55+865C=
NM_003122.4:c.55+865C= NP_003113.2:n.55+865C=
NM_001354966.1:c.55+865C= NP_001341895.1:n.55+865C=
NM_001354966.2:c.55+865C= NP_001341895.1:n.55+865C=
NM_001379610.1:c.55+865C= MANE Select NP_001366539.1:n.55+865C=
NM_003122.5:c.55+865C= NP_003113.2:n.55+865C=
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