Canonical Allele Identifier: CA128923766

Gene: SPINK5

Linked Data

• dbSNP Id: rs202082729
• MyVariant Identifiers: chr5:g.147487001del (hg19) ; chr5:g.148107438del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107438del , CM000667.2:g.148107438del	GRCh38
NC_000005.9:g.147487001del , CM000667.1:g.147487001del	GRCh37
NC_000005.8:g.147467194del	NCBI36
NG_009633.1:g.48467del , LRG_110:g.48467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1216+274del
ENST00000256084.8:c.1607+274del MANE Select	ENSP00000256084.7:n.1607+274del
ENST00000256084.7:c.1607+274del	ENSP00000256084.7:n.1607+274del
ENST00000359874.7:c.1607+274del	ENSP00000352936.3:n.1607+274del
ENST00000398454.5:c.1607+274del	ENSP00000381472.1:n.1607+274del
ENST00000507988.5:n.1771+274del
ENST00000508733.5:c.1550+274del	ENSP00000421519.1:n.1550+274del
NM_001127698.1:c.1607+274del	NP_001121170.1:n.1607+274del
NM_001127699.1:c.1607+274del	NP_001121171.1:n.1607+274del
NM_006846.3:c.1607+274del , LRG_110t1:c.1607+274del	NP_006837.2:n.1607+274del
XM_011537550.1:c.1550+274del	XP_011535852.1:n.1550+274del
XM_011537551.1:c.1523+274del	XP_011535853.1:n.1523+274del
XM_011537551.2:c.1523+274del	XP_011535853.1:n.1523+274del
NM_001127698.2:c.1607+274del	NP_001121170.1:n.1607+274del
NM_001127699.2:c.1607+274del	NP_001121171.1:n.1607+274del
NM_006846.4:c.1607+274del MANE Select	NP_006837.2:n.1607+274del