Canonical Allele Identifier: CA1589902857
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131220T= , CM000667.2:g.148131220T= GRCh38
NC_000005.9:g.147510783T= , CM000667.1:g.147510783T= GRCh37
NC_000005.8:g.147490976T= NCBI36
NG_009633.1:g.72249T= , LRG_110:g.72249T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2965-39T= MANE Select ENSP00000256084.7:n.2965-39T=
ENST00000256084.7:c.2965-39T= ENSP00000256084.7:n.2965-39T=
ENST00000359874.7:c.3055-39T= ENSP00000352936.3:n.3055-39T=
NM_001127698.1:c.3055-39T= NP_001121170.1:n.3055-39T=
NM_006846.3:c.2965-39T= , LRG_110t1:c.2965-39T= NP_006837.2:n.2965-39T=
XM_011537550.1:c.2998-39T= XP_011535852.1:n.2998-39T=
XM_011537551.1:c.2971-39T= XP_011535853.1:n.2971-39T=
XM_011537551.2:c.2971-39T= XP_011535853.1:n.2971-39T=
NM_001127698.2:c.3055-39T= NP_001121170.1:n.3055-39T=
NM_006846.4:c.2965-39T= MANE Select NP_006837.2:n.2965-39T=