Canonical Allele Identifier: CA2675856425

Gene: SPINK5

Linked Data

• gnomAD v4: 5-148106987-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148106988del , CM000667.2:g.148106988del	GRCh38
NC_000005.9:g.147486551del , CM000667.1:g.147486551del	GRCh37
NC_000005.8:g.147466744del	NCBI36
NG_009633.1:g.48017del , LRG_110:g.48017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1089-49del
ENST00000256084.8:c.1480-49del MANE Select	ENSP00000256084.7:n.1480-49del
ENST00000256084.7:c.1480-49del	ENSP00000256084.7:n.1480-49del
ENST00000359874.7:c.1480-49del	ENSP00000352936.3:n.1480-49del
ENST00000398454.5:c.1480-49del	ENSP00000381472.1:n.1480-49del
ENST00000507988.5:n.1644-49del
ENST00000508733.5:c.1423-49del	ENSP00000421519.1:n.1423-49del
NM_001127698.1:c.1480-49del	NP_001121170.1:n.1480-49del
NM_001127699.1:c.1480-49del	NP_001121171.1:n.1480-49del
NM_006846.3:c.1480-49del , LRG_110t1:c.1480-49del	NP_006837.2:n.1480-49del
XM_011537550.1:c.1423-49del	XP_011535852.1:n.1423-49del
XM_011537551.1:c.1396-49del	XP_011535853.1:n.1396-49del
XM_011537551.2:c.1396-49del	XP_011535853.1:n.1396-49del
NM_001127698.2:c.1480-49del	NP_001121170.1:n.1480-49del
NM_001127699.2:c.1480-49del	NP_001121171.1:n.1480-49del
NM_006846.4:c.1480-49del MANE Select	NP_006837.2:n.1480-49del