Canonical Allele Identifier: CA1642566893

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83517159_83517163delinsCTCTA , CM000668.2:g.83517159_83517163delinsCTCTA	GRCh38
NC_000006.11:g.84226878_84226882delinsCTCTA , CM000668.1:g.84226878_84226882delinsCTCTA	GRCh37
NC_000006.10:g.84283597_84283601delinsCTCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4465_-21+4469delinsCTCTA MANE Select	ENSP00000358714.3:n.-21+4465_-21+4469delinsCTCTA
ENST00000369700.3:c.-21+4465_-21+4469delinsCTCTA	ENSP00000358714.3:n.-21+4465_-21+4469delinsCTCTA
NM_001170423.1:c.-125-4376_-125-4372delinsCTCTA	NP_001163894.1:n.-125-4376_-125-4372delinsCTCTA
NM_153362.2:c.-21+4465_-21+4469delinsCTCTA	NP_699193.2:n.-21+4465_-21+4469delinsCTCTA
NM_153362.3:c.-21+4465_-21+4469delinsCTCTA MANE Select	NP_699193.2:n.-21+4465_-21+4469delinsCTCTA
NM_001170423.2:c.-125-4376_-125-4372delinsCTCTA	NP_001163894.1:n.-125-4376_-125-4372delinsCTCTA