Canonical Allele Identifier: CA1589902909
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131313C= , CM000667.2:g.148131313C= GRCh38
NC_000005.9:g.147510876C= , CM000667.1:g.147510876C= GRCh37
NC_000005.8:g.147491069C= NCBI36
NG_009633.1:g.72342C= , LRG_110:g.72342C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.3019C= MANE Select ENSP00000256084.7:p.Pro1007=
ENST00000256084.7:c.3019C= ENSP00000256084.7:p.Pro1007=
ENST00000359874.7:c.3109C= ENSP00000352936.3:p.Pro1037=
NM_001127698.1:c.3109C= NP_001121170.1:p.Pro1037=
NM_006846.3:c.3019C= , LRG_110t1:c.3019C= NP_006837.2:p.Pro1007=
XM_011537550.1:c.3052C= XP_011535852.1:p.Pro1018=
XM_011537551.1:c.3025C= XP_011535853.1:p.Pro1009=
XM_011537551.2:c.3025C= XP_011535853.1:p.Pro1009=
NM_001127698.2:c.3109C= NP_001121170.1:p.Pro1037=
NM_006846.4:c.3019C= MANE Select NP_006837.2:p.Pro1007=