Canonical Allele Identifier: CA563525799
Community Standard Title: NM_006846.4(SPINK5):c.2964+14T>G
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148127093T>G , CM000667.2:g.148127093T>G GRCh38
NC_000005.9:g.147506656T>G , CM000667.1:g.147506656T>G GRCh37
NC_000005.8:g.147486849T>G NCBI36
NG_009633.1:g.68122T>G , LRG_110:g.68122T>G

Transcript Alleles

HGVS Amino-acid Change
NM_006846.4:c.2964+14T>G MANE Select NP_006837.2:n.2964+14T>G
ENST00000256084.8:c.2964+14T>G MANE Select ENSP00000256084.7:n.2964+14T>G
NM_001127698.1:c.3054+14T>G NP_001121170.1:n.3054+14T>G
NM_001127698.2:c.3054+14T>G NP_001121170.1:n.3054+14T>G
NM_006846.3:c.2964+14T>G , LRG_110t1:c.2964+14T>G NP_006837.2:n.2964+14T>G
ENST00000256084.7:c.2964+14T>G ENSP00000256084.7:n.2964+14T>G
ENST00000359874.7:c.3054+14T>G ENSP00000352936.3:n.3054+14T>G
XM_011537550.1:c.2997+14T>G XP_011535852.1:n.2997+14T>G
XM_011537551.1:c.2970+14T>G XP_011535853.1:n.2970+14T>G
XM_011537551.2:c.2970+14T>G XP_011535853.1:n.2970+14T>G