Canonical Allele Identifier: CA1589892177
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148107076A= , CM000667.2:g.148107076A= GRCh38
NC_000005.9:g.147486639A= , CM000667.1:g.147486639A= GRCh37
NC_000005.8:g.147466832A= NCBI36
NG_009633.1:g.48105A= , LRG_110:g.48105A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481286.6:n.1128A=
ENST00000256084.8:c.1519A= MANE Select ENSP00000256084.7:p.Thr507=
ENST00000256084.7:c.1519A= ENSP00000256084.7:p.Thr507=
ENST00000359874.7:c.1519A= ENSP00000352936.3:p.Thr507=
ENST00000398454.5:c.1519A= ENSP00000381472.1:p.Thr507=
ENST00000507988.5:n.1683A=
ENST00000508733.5:c.1462A= ENSP00000421519.1:p.Thr488=
NM_001127698.1:c.1519A= NP_001121170.1:p.Thr507=
NM_001127699.1:c.1519A= NP_001121171.1:p.Thr507=
NM_006846.3:c.1519A= , LRG_110t1:c.1519A= NP_006837.2:p.Thr507=
XM_011537550.1:c.1462A= XP_011535852.1:p.Thr488=
XM_011537551.1:c.1435A= XP_011535853.1:p.Thr479=
XM_011537551.2:c.1435A= XP_011535853.1:p.Thr479=
NM_001127698.2:c.1519A= NP_001121170.1:p.Thr507=
NM_001127699.2:c.1519A= NP_001121171.1:p.Thr507=
NM_006846.4:c.1519A= MANE Select NP_006837.2:p.Thr507=