Canonical Allele Identifier: CA1335307978

Gene: PRSS56

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523593_232523594delinsTC , CM000664.2:g.232523593_232523594delinsTC	GRCh38
NC_000002.11:g.233388303_233388304delinsTC , CM000664.1:g.233388303_233388304delinsTC	GRCh37
NC_000002.10:g.233096547_233096548delinsTC	NCBI36
NG_008028.1:g.2382_2383delinsTC
NG_031969.1:g.8131_8132delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1012+15_1012+16delinsTC MANE Select	ENSP00000479745.1:n.1012+15_1012+16delinsTC
ENST00000449534.6:c.1012+15_1012+16delinsTC	ENSP00000473410.1:n.1012+15_1012+16delinsTC
ENST00000617714.1:c.1012+15_1012+16delinsTC	ENSP00000479745.1:n.1012+15_1012+16delinsTC
NM_001195129.1:c.1012+15_1012+16delinsTC	NP_001182058.1:n.1012+15_1012+16delinsTC
NM_001195129.2:c.1012+15_1012+16delinsTC MANE Select	NP_001182058.1:n.1012+15_1012+16delinsTC
NM_001369848.1:c.1012+15_1012+16delinsTC	NP_001356777.1:n.1012+15_1012+16delinsTC