Canonical Allele Identifier: CA1589902898
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131296G= , CM000667.2:g.148131296G= GRCh38
NC_000005.9:g.147510859G= , CM000667.1:g.147510859G= GRCh37
NC_000005.8:g.147491052G= NCBI36
NG_009633.1:g.72325G= , LRG_110:g.72325G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.3002G= MANE Select ENSP00000256084.7:p.Arg1001=
ENST00000256084.7:c.3002G= ENSP00000256084.7:p.Arg1001=
ENST00000359874.7:c.3092G= ENSP00000352936.3:p.Arg1031=
NM_001127698.1:c.3092G= NP_001121170.1:p.Arg1031=
NM_006846.3:c.3002G= , LRG_110t1:c.3002G= NP_006837.2:p.Arg1001=
XM_011537550.1:c.3035G= XP_011535852.1:p.Arg1012=
XM_011537551.1:c.3008G= XP_011535853.1:p.Arg1003=
XM_011537551.2:c.3008G= XP_011535853.1:p.Arg1003=
NM_001127698.2:c.3092G= NP_001121170.1:p.Arg1031=
NM_006846.4:c.3002G= MANE Select NP_006837.2:p.Arg1001=