Canonical Allele Identifier: CA1589902893
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131287T= , CM000667.2:g.148131287T= GRCh38
NC_000005.9:g.147510850T= , CM000667.1:g.147510850T= GRCh37
NC_000005.8:g.147491043T= NCBI36
NG_009633.1:g.72316T= , LRG_110:g.72316T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2993T= MANE Select ENSP00000256084.7:p.Val998=
ENST00000256084.7:c.2993T= ENSP00000256084.7:p.Val998=
ENST00000359874.7:c.3083T= ENSP00000352936.3:p.Val1028=
NM_001127698.1:c.3083T= NP_001121170.1:p.Val1028=
NM_006846.3:c.2993T= , LRG_110t1:c.2993T= NP_006837.2:p.Val998=
XM_011537550.1:c.3026T= XP_011535852.1:p.Val1009=
XM_011537551.1:c.2999T= XP_011535853.1:p.Val1000=
XM_011537551.2:c.2999T= XP_011535853.1:p.Val1000=
NM_001127698.2:c.3083T= NP_001121170.1:p.Val1028=
NM_006846.4:c.2993T= MANE Select NP_006837.2:p.Val998=