Canonical Allele Identifier: CA361651876
Gene: SPINK5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131263C>A , CM000667.2:g.148131263C>A GRCh38
NC_000005.9:g.147510826C>A , CM000667.1:g.147510826C>A GRCh37
NC_000005.8:g.147491019C>A NCBI36
NG_009633.1:g.72292C>A , LRG_110:g.72292C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2969C>A MANE Select ENSP00000256084.7:p.Ser990Tyr
ENST00000256084.7:c.2969C>A ENSP00000256084.7:p.Ser990Tyr
ENST00000359874.7:c.3059C>A ENSP00000352936.3:p.Ser1020Tyr
NM_001127698.1:c.3059C>A NP_001121170.1:p.Ser1020Tyr
NM_006846.3:c.2969C>A , LRG_110t1:c.2969C>A NP_006837.2:p.Ser990Tyr
XM_011537550.1:c.3002C>A XP_011535852.1:p.Ser1001Tyr
XM_011537551.1:c.2975C>A XP_011535853.1:p.Ser992Tyr
XM_011537551.2:c.2975C>A XP_011535853.1:p.Ser992Tyr
NM_001127698.2:c.3059C>A NP_001121170.1:p.Ser1020Tyr
NM_006846.4:c.2969C>A MANE Select NP_006837.2:p.Ser990Tyr