Canonical Allele Identifier: CA1589902921
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131343G= , CM000667.2:g.148131343G= GRCh38
NC_000005.9:g.147510906G= , CM000667.1:g.147510906G= GRCh37
NC_000005.8:g.147491099G= NCBI36
NG_009633.1:g.72372G= , LRG_110:g.72372G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.3049G= MANE Select ENSP00000256084.7:p.Asp1017=
ENST00000256084.7:c.3049G= ENSP00000256084.7:p.Asp1017=
ENST00000359874.7:c.3139G= ENSP00000352936.3:p.Asp1047=
NM_001127698.1:c.3139G= NP_001121170.1:p.Asp1047=
NM_006846.3:c.3049G= , LRG_110t1:c.3049G= NP_006837.2:p.Asp1017=
XM_011537550.1:c.3082G= XP_011535852.1:p.Asp1028=
XM_011537551.1:c.3055G= XP_011535853.1:p.Asp1019=
XM_011537551.2:c.3055G= XP_011535853.1:p.Asp1019=
NM_001127698.2:c.3139G= NP_001121170.1:p.Asp1047=
NM_006846.4:c.3049G= MANE Select NP_006837.2:p.Asp1017=