Canonical Allele Identifier: CA1589902891
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131284G= , CM000667.2:g.148131284G= GRCh38
NC_000005.9:g.147510847G= , CM000667.1:g.147510847G= GRCh37
NC_000005.8:g.147491040G= NCBI36
NG_009633.1:g.72313G= , LRG_110:g.72313G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2990G= MANE Select ENSP00000256084.7:p.Arg997=
ENST00000256084.7:c.2990G= ENSP00000256084.7:p.Arg997=
ENST00000359874.7:c.3080G= ENSP00000352936.3:p.Arg1027=
NM_001127698.1:c.3080G= NP_001121170.1:p.Arg1027=
NM_006846.3:c.2990G= , LRG_110t1:c.2990G= NP_006837.2:p.Arg997=
XM_011537550.1:c.3023G= XP_011535852.1:p.Arg1008=
XM_011537551.1:c.2996G= XP_011535853.1:p.Arg999=
XM_011537551.2:c.2996G= XP_011535853.1:p.Arg999=
NM_001127698.2:c.3080G= NP_001121170.1:p.Arg1027=
NM_006846.4:c.2990G= MANE Select NP_006837.2:p.Arg997=