Canonical Allele Identifier: CA458522929

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142458443G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142750592G>T , CM000669.2:g.142750592G>T	GRCh38
NC_000007.13:g.142458443G>T , CM000669.1:g.142458443G>T	GRCh37
NC_000007.12:g.142138017G>T	NCBI36
NG_008307.3:g.6109G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000311737.12:c.78G>T (PRSS1) MANE Select	ENSP00000308720.7:p.Gly26=
ENST00000311737.11:c.78G>T (PRSS1)	ENSP00000308720.7:p.Gly26=
ENST00000485223.1:n.54-37G>T (PRSS1)
ENST00000486171.5:c.78G>T (PRSS1)	ENSP00000417854.1:p.Gly26=
ENST00000497041.1:n.82G>T (PRSS1)
ENST00000610416.2:c.370+29406G>T (TRBC1)	ENSP00000482915.1:n.370+29406G>T
ENST00000612126.4:c.78G>T (PRSS1)	ENSP00000479959.1:p.Gly26=
ENST00000619214.4:c.78G>T (PRSS1)	ENSP00000481361.1:p.Gly26=
ENST00000633114.1:c.78G>T (PRSS2)	ENSP00000487822.1:p.Gly26=
ENST00000634019.1:c.82+1801G>T (PRSS2)	ENSP00000488594.1:n.82+1801G>T
NM_002769.4:c.78G>T (PRSS1)	NP_002760.1:p.Gly26=
XM_011516411.1:c.753G>T (PRSS1)	XP_011514713.1:p.Gly251=
NM_002769.5:c.78G>T (PRSS1) MANE Select	NP_002760.1:p.Gly26=
NR_172947.1:n.91G>T (PRSS1)
NR_172948.1:n.91G>T (PRSS1)
NR_172949.1:n.54-37G>T (PRSS1)
NR_172950.1:n.53+1068G>T (PRSS1)
NR_172951.1:n.54-37G>T (PRSS1)