Canonical Allele Identifier: CA913189665
Community Standard Title: NM_006846.4(SPINK5):c.795-11A>G
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148095807A>G , CM000667.2:g.148095807A>G GRCh38
NC_000005.9:g.147475370A>G , CM000667.1:g.147475370A>G GRCh37
NC_000005.8:g.147455563A>G NCBI36
NG_009633.1:g.36836A>G , LRG_110:g.36836A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006846.4:c.795-11A>G MANE Select NP_006837.2:n.795-11A>G
ENST00000256084.8:c.795-11A>G MANE Select ENSP00000256084.7:n.795-11A>G
NM_001127698.1:c.795-11A>G NP_001121170.1:n.795-11A>G
NM_001127698.2:c.795-11A>G NP_001121170.1:n.795-11A>G
NM_001127699.1:c.795-11A>G NP_001121171.1:n.795-11A>G
NM_001127699.2:c.795-11A>G NP_001121171.1:n.795-11A>G
NM_006846.3:c.795-11A>G , LRG_110t1:c.795-11A>G NP_006837.2:n.795-11A>G
ENST00000256084.7:c.795-11A>G ENSP00000256084.7:n.795-11A>G
ENST00000359874.7:c.795-11A>G ENSP00000352936.3:n.795-11A>G
ENST00000398454.5:c.795-11A>G ENSP00000381472.1:n.795-11A>G
ENST00000476608.1:n.311-11A>G
ENST00000476697.7:c.*320-11A>G ENSP00000427943.1:n.*320-11A>G
ENST00000481286.5:n.241-11A>G
ENST00000481286.6:n.404-11A>G
ENST00000507988.5:n.959-11A>G
ENST00000508733.5:c.738-11A>G ENSP00000421519.1:n.738-11A>G
ENST00000698105.1:n.665-11A>G
XM_011537550.1:c.738-11A>G XP_011535852.1:n.738-11A>G
XM_011537551.1:c.711-11A>G XP_011535853.1:n.711-11A>G
XM_011537551.2:c.711-11A>G XP_011535853.1:n.711-11A>G