Canonical Allele Identifier: CA3495480
Community Standard Title: NM_006846.4(SPINK5):c.1093-4G>A
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148100450G>A , CM000667.2:g.148100450G>A GRCh38
NC_000005.9:g.147480013G>A , CM000667.1:g.147480013G>A GRCh37
NC_000005.8:g.147460206G>A NCBI36
NG_009633.1:g.41479G>A , LRG_110:g.41479G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006846.4:c.1093-4G>A MANE Select NP_006837.2:n.1093-4G>A
ENST00000256084.8:c.1093-4G>A MANE Select ENSP00000256084.7:n.1093-4G>A
NM_001127698.1:c.1093-4G>A NP_001121170.1:n.1093-4G>A
NM_001127698.2:c.1093-4G>A NP_001121170.1:n.1093-4G>A
NM_001127699.1:c.1093-4G>A NP_001121171.1:n.1093-4G>A
NM_001127699.2:c.1093-4G>A NP_001121171.1:n.1093-4G>A
NM_006846.3:c.1093-4G>A , LRG_110t1:c.1093-4G>A NP_006837.2:n.1093-4G>A
ENST00000256084.7:c.1093-4G>A ENSP00000256084.7:n.1093-4G>A
ENST00000359874.7:c.1093-4G>A ENSP00000352936.3:n.1093-4G>A
ENST00000398454.5:c.1093-4G>A ENSP00000381472.1:n.1093-4G>A
ENST00000476608.1:n.609-4G>A
ENST00000481286.6:n.702-4G>A
ENST00000507988.5:n.1257-4G>A
ENST00000508733.5:c.1036-4G>A ENSP00000421519.1:n.1036-4G>A
XM_011537550.1:c.1036-4G>A XP_011535852.1:n.1036-4G>A
XM_011537551.1:c.1009-4G>A XP_011535853.1:n.1009-4G>A
XM_011537551.2:c.1009-4G>A XP_011535853.1:n.1009-4G>A