Canonical Allele Identifier: CA1082736749
Gene: SPINK5 HGNC NCBI

Linked Data

dbSNP Id: rs1754561307

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131210del , CM000667.2:g.148131210del GRCh38
NC_000005.9:g.147510773del , CM000667.1:g.147510773del GRCh37
NC_000005.8:g.147490966del NCBI36
NG_009633.1:g.72239del , LRG_110:g.72239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2965-49del MANE Select ENSP00000256084.7:n.2965-49del
ENST00000256084.7:c.2965-49del ENSP00000256084.7:n.2965-49del
ENST00000359874.7:c.3055-49del ENSP00000352936.3:n.3055-49del
NM_001127698.1:c.3055-49del NP_001121170.1:n.3055-49del
NM_006846.3:c.2965-49del , LRG_110t1:c.2965-49del NP_006837.2:n.2965-49del
XM_011537550.1:c.2998-49del XP_011535852.1:n.2998-49del
XM_011537551.1:c.2971-49del XP_011535853.1:n.2971-49del
XM_011537551.2:c.2971-49del XP_011535853.1:n.2971-49del
NM_001127698.2:c.3055-49del NP_001121170.1:n.3055-49del
NM_006846.4:c.2965-49del MANE Select NP_006837.2:n.2965-49del