Canonical Allele Identifier: CA1589902885
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131264T= , CM000667.2:g.148131264T= GRCh38
NC_000005.9:g.147510827T= , CM000667.1:g.147510827T= GRCh37
NC_000005.8:g.147491020T= NCBI36
NG_009633.1:g.72293T= , LRG_110:g.72293T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2970T= MANE Select ENSP00000256084.7:p.Ser990=
ENST00000256084.7:c.2970T= ENSP00000256084.7:p.Ser990=
ENST00000359874.7:c.3060T= ENSP00000352936.3:p.Ser1020=
NM_001127698.1:c.3060T= NP_001121170.1:p.Ser1020=
NM_006846.3:c.2970T= , LRG_110t1:c.2970T= NP_006837.2:p.Ser990=
XM_011537550.1:c.3003T= XP_011535852.1:p.Ser1001=
XM_011537551.1:c.2976T= XP_011535853.1:p.Ser992=
XM_011537551.2:c.2976T= XP_011535853.1:p.Ser992=
NM_001127698.2:c.3060T= NP_001121170.1:p.Ser1020=
NM_006846.4:c.2970T= MANE Select NP_006837.2:p.Ser990=