Canonical Allele Identifier: CA361644672
Gene: SPINK5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148118458G>T , CM000667.2:g.148118458G>T GRCh38
NC_000005.9:g.147498021G>T , CM000667.1:g.147498021G>T GRCh37
NC_000005.8:g.147478214G>T NCBI36
NG_009633.1:g.59487G>T , LRG_110:g.59487G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2134G>T MANE Select ENSP00000256084.7:p.Glu712Ter
ENST00000256084.7:c.2134G>T ENSP00000256084.7:p.Glu712Ter
ENST00000359874.7:c.2134G>T ENSP00000352936.3:p.Glu712Ter
ENST00000398454.5:c.2134G>T ENSP00000381472.1:p.Glu712Ter
ENST00000507988.5:n.2298G>T
ENST00000508733.5:c.2077G>T ENSP00000421519.1:p.Glu693Ter
NM_001127698.1:c.2134G>T NP_001121170.1:p.Glu712Ter
NM_001127699.1:c.2134G>T NP_001121171.1:p.Glu712Ter
NM_006846.3:c.2134G>T , LRG_110t1:c.2134G>T NP_006837.2:p.Glu712Ter
XM_011537550.1:c.2077G>T XP_011535852.1:p.Glu693Ter
XM_011537551.1:c.2050G>T XP_011535853.1:p.Glu684Ter
XM_011537551.2:c.2050G>T XP_011535853.1:p.Glu684Ter
NM_001127698.2:c.2134G>T NP_001121170.1:p.Glu712Ter
NM_001127699.2:c.2134G>T NP_001121171.1:p.Glu712Ter
NM_006846.4:c.2134G>T MANE Select NP_006837.2:p.Glu712Ter