Canonical Allele Identifier: CA2519544449

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752348C>A , CM000669.2:g.142752348C>A GRCh38
NC_000007.13:g.142460199C>A , CM000669.1:g.142460199C>A GRCh37
NC_000007.12:g.142139773C>A NCBI36
NG_008307.3:g.7865C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.455-83C>A (PRSS1) MANE Select ENSP00000308720.7:n.455-83C>A
ENST00000311737.11:c.455-83C>A (PRSS1) ENSP00000308720.7:n.455-83C>A
ENST00000463701.1:n.919-83C>A (PRSS1)
ENST00000486171.5:c.497-83C>A (PRSS1) ENSP00000417854.1:n.497-83C>A
ENST00000492062.1:c.305-83C>A (PRSS1) ENSP00000419912.1:n.305-83C>A
ENST00000610416.2:c.370+31162C>A (TRBC1) ENSP00000482915.1:n.370+31162C>A
ENST00000612126.4:c.455-83C>A (PRSS1) ENSP00000479959.1:n.455-83C>A
ENST00000619214.4:c.425-83C>A (PRSS1) ENSP00000481361.1:n.425-83C>A
ENST00000633114.1:c.321+454C>A (PRSS2) ENSP00000487822.1:n.321+454C>A
ENST00000634019.1:c.82+3557C>A (PRSS2) ENSP00000488594.1:n.82+3557C>A
NM_002769.4:c.455-83C>A (PRSS1) NP_002760.1:n.455-83C>A
XM_011516411.1:c.1130-83C>A (PRSS1) XP_011514713.1:n.1130-83C>A
NM_002769.5:c.455-83C>A (PRSS1) MANE Select NP_002760.1:n.455-83C>A
NR_172947.1:n.397-83C>A (PRSS1)
NR_172948.1:n.394-83C>A (PRSS1)
NR_172949.1:n.394-83C>A (PRSS1)
NR_172950.1:n.308-83C>A (PRSS1)
NR_172951.1:n.242-83C>A (PRSS1)