Canonical Allele Identifier: CA1589892246
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148107235T= , CM000667.2:g.148107235T= GRCh38
NC_000005.9:g.147486798T= , CM000667.1:g.147486798T= GRCh37
NC_000005.8:g.147466991T= NCBI36
NG_009633.1:g.48264T= , LRG_110:g.48264T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481286.6:n.1216+71T=
ENST00000256084.8:c.1607+71T= MANE Select ENSP00000256084.7:n.1607+71T=
ENST00000256084.7:c.1607+71T= ENSP00000256084.7:n.1607+71T=
ENST00000359874.7:c.1607+71T= ENSP00000352936.3:n.1607+71T=
ENST00000398454.5:c.1607+71T= ENSP00000381472.1:n.1607+71T=
ENST00000507988.5:n.1771+71T=
ENST00000508733.5:c.1550+71T= ENSP00000421519.1:n.1550+71T=
NM_001127698.1:c.1607+71T= NP_001121170.1:n.1607+71T=
NM_001127699.1:c.1607+71T= NP_001121171.1:n.1607+71T=
NM_006846.3:c.1607+71T= , LRG_110t1:c.1607+71T= NP_006837.2:n.1607+71T=
XM_011537550.1:c.1550+71T= XP_011535852.1:n.1550+71T=
XM_011537551.1:c.1523+71T= XP_011535853.1:n.1523+71T=
XM_011537551.2:c.1523+71T= XP_011535853.1:n.1523+71T=
NM_001127698.2:c.1607+71T= NP_001121170.1:n.1607+71T=
NM_001127699.2:c.1607+71T= NP_001121171.1:n.1607+71T=
NM_006846.4:c.1607+71T= MANE Select NP_006837.2:n.1607+71T=