Canonical Allele Identifier: CA394419462

Gene: PRSS21

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2818760C>A , CM000678.2:g.2818760C>A	GRCh38
NC_000016.9:g.2868761C>A , CM000678.1:g.2868761C>A	GRCh37
NC_000016.8:g.2808762C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006799.4:c.341C>A MANE Select	NP_006790.1:p.Ala114Asp
ENST00000005995.8:c.341C>A MANE Select	ENSP00000005995.3:p.Ala114Asp
NM_001270452.1:c.335C>A	NP_001257381.1:p.Ala112Asp
NM_001270452.2:c.335C>A	NP_001257381.1:p.Ala112Asp
NM_006799.3:c.341C>A	NP_006790.1:p.Ala114Asp
NM_144956.2:c.335C>A	NP_659205.1:p.Ala112Asp
NM_144956.3:c.335C>A	NP_659205.1:p.Ala112Asp
NM_144957.2:c.341C>A	NP_659206.1:p.Ala114Asp
NM_144957.3:c.341C>A	NP_659206.1:p.Ala114Asp
NR_073012.1:n.365C>A
NR_073012.2:n.291C>A
ENST00000005995.7:c.341C>A	ENSP00000005995.3:p.Ala114Asp
ENST00000450020.7:c.341C>A	ENSP00000407741.3:p.Ala114Asp
ENST00000570594.5:c.331C>A
ENST00000570629.5:c.251C>A	ENSP00000460417.1:n.251C>A
ENST00000574265.1:c.166C>A
ENST00000574813.5:c.313C>A
ENST00000575199.1:n.360C>A
ENST00000577043.1:n.372C>A
XM_017022875.1:c.335C>A	XP_016878364.1:p.Ala112Asp
XM_017022876.1:c.341C>A	XP_016878365.1:p.Ala114Asp
XM_017022877.1:c.335C>A	XP_016878366.1:p.Ala112Asp
XM_017022878.1:c.341C>A	XP_016878367.1:p.Ala114Asp