Canonical Allele Identifier: CA1589888383
Community Standard Title: NM_006846.4(SPINK5):c.1103G= (p.Ser368=)
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148100464G= , CM000667.2:g.148100464G= GRCh38
NC_000005.9:g.147480027G= , CM000667.1:g.147480027G= GRCh37
NC_000005.8:g.147460220G= NCBI36
NG_009633.1:g.41493G= , LRG_110:g.41493G=

Transcript Alleles

HGVS Amino-acid Change
NM_006846.4:c.1103G= MANE Select NP_006837.2:p.Ser368=
ENST00000256084.8:c.1103G= MANE Select ENSP00000256084.7:p.Ser368=
NM_001127698.1:c.1103G= NP_001121170.1:p.Ser368=
NM_001127698.2:c.1103G= NP_001121170.1:p.Ser368=
NM_001127699.1:c.1103G= NP_001121171.1:p.Ser368=
NM_001127699.2:c.1103G= NP_001121171.1:p.Ser368=
NM_006846.3:c.1103G= , LRG_110t1:c.1103G= NP_006837.2:p.Ser368=
ENST00000256084.7:c.1103G= ENSP00000256084.7:p.Ser368=
ENST00000359874.7:c.1103G= ENSP00000352936.3:p.Ser368=
ENST00000398454.5:c.1103G= ENSP00000381472.1:p.Ser368=
ENST00000476608.1:n.619G=
ENST00000481286.6:n.712G=
ENST00000507988.5:n.1267G=
ENST00000508733.5:c.1046G= ENSP00000421519.1:p.Ser349=
XM_011537550.1:c.1046G= XP_011535852.1:p.Ser349=
XM_011537551.1:c.1019G= XP_011535853.1:p.Ser340=
XM_011537551.2:c.1019G= XP_011535853.1:p.Ser340=