Canonical Allele Identifier: CA236323579
Gene: CELA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51333812C>T , CM000674.2:g.51333812C>T GRCh38
NC_000012.11:g.51727596C>T , CM000674.1:g.51727596C>T GRCh37
NC_000012.10:g.50013863C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293636.2:c.610-3979G>A MANE Select ENSP00000293636.1:n.610-3979G>A
ENST00000293636.1:c.610-3979G>A ENSP00000293636.1:n.610-3979G>A
NM_001971.5:c.610-3979G>A NP_001962.3:n.610-3979G>A
NM_001971.6:c.610-3979G>A MANE Select NP_001962.3:n.610-3979G>A