Canonical Allele Identifier: CA1589902882
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131260A= , CM000667.2:g.148131260A= GRCh38
NC_000005.9:g.147510823A= , CM000667.1:g.147510823A= GRCh37
NC_000005.8:g.147491016A= NCBI36
NG_009633.1:g.72289A= , LRG_110:g.72289A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2966A= MANE Select ENSP00000256084.7:p.Asp989=
ENST00000256084.7:c.2966A= ENSP00000256084.7:p.Asp989=
ENST00000359874.7:c.3056A= ENSP00000352936.3:p.Asp1019=
NM_001127698.1:c.3056A= NP_001121170.1:p.Asp1019=
NM_006846.3:c.2966A= , LRG_110t1:c.2966A= NP_006837.2:p.Asp989=
XM_011537550.1:c.2999A= XP_011535852.1:p.Asp1000=
XM_011537551.1:c.2972A= XP_011535853.1:p.Asp991=
XM_011537551.2:c.2972A= XP_011535853.1:p.Asp991=
NM_001127698.2:c.3056A= NP_001121170.1:p.Asp1019=
NM_006846.4:c.2966A= MANE Select NP_006837.2:p.Asp989=