Canonical Allele Identifier: CA2587779669

Gene: PRSS57

Linked Data

• gnomAD v4: 19-694985-TGAGTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694987_694992del , CM000681.2:g.694987_694992del	GRCh38
NC_000019.9:g.694987_694992del , CM000681.1:g.694987_694992del	GRCh37
NC_000019.8:g.645987_645992del	NCBI36
NG_051189.1:g.5541_5546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-24_80-19del MANE Select	ENSP00000327386.6:n.80-24_80-19del
ENST00000329267.8:c.80-24_80-19del	ENSP00000327386.6:n.80-24_80-19del
ENST00000613411.4:c.80-21_80-16del	ENSP00000482358.1:n.80-21_80-16del
NM_001308209.1:c.80-24_80-19del	NP_001295138.1:n.80-24_80-19del
NM_214710.3:c.80-21_80-16del	NP_999875.1:n.80-21_80-16del
NM_214710.4:c.80-21_80-16del	NP_999875.1:n.80-21_80-16del
NM_001308209.2:c.80-24_80-19del MANE Select	NP_001295138.2:n.80-24_80-19del
NM_214710.5:c.80-21_80-16del	NP_999875.2:n.80-21_80-16del