Canonical Allele Identifier: CA2685351413

Gene: PRSS2 TRBC1

Linked Data

• gnomAD v4: 7-142774097-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774097C>T , CM000669.2:g.142774097C>T	GRCh38
NC_000007.13:g.142481957C>T , CM000669.1:g.142481957C>T	GRCh37
NC_000007.12:g.142181900C>T	NCBI36
NG_008322.2:g.8155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.591+42C>T (PRSS2) MANE Select	ENSP00000488338.1:n.591+42C>T
ENST00000539842.5:c.591+42C>T (PRSS2)	ENSP00000488338.1:n.591+42C>T
ENST00000610416.2:c.371-12941C>T (TRBC1)	ENSP00000482915.1:n.371-12941C>T
ENST00000618750.2:n.424+59C>T (PRSS2)
ENST00000632805.1:c.588+42C>T (PRSS2)	ENSP00000488077.1:n.588+42C>T
ENST00000632998.1:c.591+42C>T (PRSS2)	ENSP00000488789.1:n.591+42C>T
ENST00000633114.1:c.597+42C>T (PRSS2)	ENSP00000487822.1:n.597+42C>T
ENST00000633969.1:c.633+42C>T (PRSS2)	ENSP00000488437.1:n.633+42C>T
ENST00000634019.1:c.633+42C>T (PRSS2)	ENSP00000488594.1:n.633+42C>T
NM_001303414.1:c.633+42C>T (PRSS2)	NP_001290343.1:n.633+42C>T
NM_002770.3:c.591+42C>T (PRSS2)	NP_002761.1:n.591+42C>T
NR_130149.1:n.557+42C>T (PRSS2)
NM_002770.4:c.591+42C>T (PRSS2) MANE Select	NP_002761.1:n.591+42C>T
NR_130149.2:n.530+42C>T (PRSS2)
NM_001303414.2:c.633+42C>T (PRSS2)	NP_001290343.1:n.633+42C>T