Canonical Allele Identifier: CA458273442

Gene: PRSS2 TRBC1

Linked Data

• MyVariant Identifiers: chr7:g.142481898A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774041A>C , CM000669.2:g.142774041A>C	GRCh38
NC_000007.13:g.142481898A>C , CM000669.1:g.142481898A>C	GRCh37
NC_000007.12:g.142181844A>C	NCBI36
NG_008322.2:g.8099A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.577A>C (PRSS2) MANE Select	ENSP00000488338.1:p.Lys193Gln
ENST00000539842.5:c.577A>C (PRSS2)	ENSP00000488338.1:p.Lys193Gln
ENST00000610416.2:c.371-12997A>C (TRBC1)	ENSP00000482915.1:n.371-12997A>C
ENST00000618750.2:n.424+3A>C (PRSS2)
ENST00000632805.1:c.574A>C (PRSS2)	ENSP00000488077.1:p.Lys192Gln
ENST00000632998.1:c.577A>C (PRSS2)	ENSP00000488789.1:p.Lys193Gln
ENST00000633114.1:c.583A>C (PRSS2)	ENSP00000487822.1:p.Lys195Gln
ENST00000633969.1:c.619A>C (PRSS2)	ENSP00000488437.1:p.Lys207Gln
ENST00000634019.1:c.619A>C (PRSS2)	ENSP00000488594.1:p.Lys207Gln
NM_001303414.1:c.619A>C (PRSS2)	NP_001290343.1:p.Lys207Gln
NM_002770.3:c.577A>C (PRSS2)	NP_002761.1:p.Lys193Gln
NR_130149.1:n.543A>C (PRSS2)
NM_002770.4:c.577A>C (PRSS2) MANE Select	NP_002761.1:p.Lys193Gln
NR_130149.2:n.516A>C (PRSS2)
NM_001303414.2:c.619A>C (PRSS2)	NP_001290343.1:p.Lys207Gln