Canonical Allele Identifier: CA361639124

Gene: SPINK5

Linked Data

• dbSNP Id: rs1436945591
• MyVariant Identifiers: chr5:g.147486623C>G (hg19) ; chr5:g.148107060C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107060C>G , CM000667.2:g.148107060C>G	GRCh38
NC_000005.9:g.147486623C>G , CM000667.1:g.147486623C>G	GRCh37
NC_000005.8:g.147466816C>G	NCBI36
NG_009633.1:g.48089C>G , LRG_110:g.48089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1112C>G
ENST00000256084.8:c.1503C>G MANE Select	ENSP00000256084.7:p.Asp501Glu
ENST00000256084.7:c.1503C>G	ENSP00000256084.7:p.Asp501Glu
ENST00000359874.7:c.1503C>G	ENSP00000352936.3:p.Asp501Glu
ENST00000398454.5:c.1503C>G	ENSP00000381472.1:p.Asp501Glu
ENST00000507988.5:n.1667C>G
ENST00000508733.5:c.1446C>G	ENSP00000421519.1:p.Asp482Glu
NM_001127698.1:c.1503C>G	NP_001121170.1:p.Asp501Glu
NM_001127699.1:c.1503C>G	NP_001121171.1:p.Asp501Glu
NM_006846.3:c.1503C>G , LRG_110t1:c.1503C>G	NP_006837.2:p.Asp501Glu
XM_011537550.1:c.1446C>G	XP_011535852.1:p.Asp482Glu
XM_011537551.1:c.1419C>G	XP_011535853.1:p.Asp473Glu
XM_011537551.2:c.1419C>G	XP_011535853.1:p.Asp473Glu
NM_001127698.2:c.1503C>G	NP_001121170.1:p.Asp501Glu
NM_001127699.2:c.1503C>G	NP_001121171.1:p.Asp501Glu
NM_006846.4:c.1503C>G MANE Select	NP_006837.2:p.Asp501Glu