Canonical Allele Identifier: CA1589902935
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131385A= , CM000667.2:g.148131385A= GRCh38
NC_000005.9:g.147510948A= , CM000667.1:g.147510948A= GRCh37
NC_000005.8:g.147491141A= NCBI36
NG_009633.1:g.72414A= , LRG_110:g.72414A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.3091A= MANE Select ENSP00000256084.7:p.Asn1031=
ENST00000256084.7:c.3091A= ENSP00000256084.7:p.Asn1031=
ENST00000359874.7:c.3181A= ENSP00000352936.3:p.Asn1061=
NM_001127698.1:c.3181A= NP_001121170.1:p.Asn1061=
NM_006846.3:c.3091A= , LRG_110t1:c.3091A= NP_006837.2:p.Asn1031=
XM_011537550.1:c.3124A= XP_011535852.1:p.Asn1042=
XM_011537551.1:c.3097A= XP_011535853.1:p.Asn1033=
XM_011537551.2:c.3097A= XP_011535853.1:p.Asn1033=
NM_001127698.2:c.3181A= NP_001121170.1:p.Asn1061=
NM_006846.4:c.3091A= MANE Select NP_006837.2:p.Asn1031=