Canonical Allele Identifier: CA2587779761

Gene: PRSS57

Linked Data

• gnomAD v4: 19-695023-TGGGGTCAGGGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695028_695039del , CM000681.2:g.695028_695039del	GRCh38
NC_000019.9:g.695028_695039del , CM000681.1:g.695028_695039del	GRCh37
NC_000019.8:g.646028_646039del	NCBI36
NG_051189.1:g.5497_5508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-68_80-57del MANE Select	ENSP00000327386.6:n.80-68_80-57del
ENST00000329267.8:c.80-68_80-57del	ENSP00000327386.6:n.80-68_80-57del
ENST00000613411.4:c.80-65_80-54del	ENSP00000482358.1:n.80-65_80-54del
NM_001308209.1:c.80-68_80-57del	NP_001295138.1:n.80-68_80-57del
NM_214710.3:c.80-65_80-54del	NP_999875.1:n.80-65_80-54del
NM_214710.4:c.80-65_80-54del	NP_999875.1:n.80-65_80-54del
NM_001308209.2:c.80-68_80-57del MANE Select	NP_001295138.2:n.80-68_80-57del
NM_214710.5:c.80-65_80-54del	NP_999875.2:n.80-65_80-54del