Canonical Allele Identifier: CA369609164

Gene: PRSS1 TRBC1 PRSS2

Linked Data

• MyVariant Identifiers: chr7:g.142459849C>A (hg19) ; chr7:g.142751998C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142751998C>A , CM000669.2:g.142751998C>A	GRCh38
NC_000007.13:g.142459849C>A , CM000669.1:g.142459849C>A	GRCh37
NC_000007.12:g.142139423C>A	NCBI36
NG_008307.3:g.7515C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311737.12:c.425C>A (PRSS1) MANE Select	ENSP00000308720.7:p.Ser142Tyr
ENST00000311737.11:c.425C>A (PRSS1)	ENSP00000308720.7:p.Ser142Tyr
ENST00000463701.1:n.889C>A (PRSS1)
ENST00000485223.1:n.1423C>A (PRSS1)
ENST00000486171.5:c.467C>A (PRSS1)	ENSP00000417854.1:p.Ser156Tyr
ENST00000492062.1:c.275C>A (PRSS1)	ENSP00000419912.1:p.Ser92Tyr
ENST00000610416.2:c.370+30812C>A (TRBC1)	ENSP00000482915.1:n.370+30812C>A
ENST00000612126.4:c.425C>A (PRSS1)	ENSP00000479959.1:p.Ser142Tyr
ENST00000619214.4:c.395C>A (PRSS1)	ENSP00000481361.1:p.Ser132Tyr
ENST00000633114.1:c.321+104C>A (PRSS2)	ENSP00000487822.1:n.321+104C>A
ENST00000634019.1:c.82+3207C>A (PRSS2)	ENSP00000488594.1:n.82+3207C>A
NM_002769.4:c.425C>A (PRSS1)	NP_002760.1:p.Ser142Tyr
XM_011516411.1:c.1100C>A (PRSS1)	XP_011514713.1:p.Ser367Tyr
NM_002769.5:c.425C>A (PRSS1) MANE Select	NP_002760.1:p.Ser142Tyr
NR_172947.1:n.367C>A (PRSS1)
NR_172948.1:n.364C>A (PRSS1)
NR_172949.1:n.364C>A (PRSS1)
NR_172950.1:n.278C>A (PRSS1)
NR_172951.1:n.212C>A (PRSS1)