Canonical Allele Identifier: CA361639165

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147486640C>G (hg19) ; chr5:g.148107077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107077C>G , CM000667.2:g.148107077C>G	GRCh38
NC_000005.9:g.147486640C>G , CM000667.1:g.147486640C>G	GRCh37
NC_000005.8:g.147466833C>G	NCBI36
NG_009633.1:g.48106C>G , LRG_110:g.48106C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1129C>G
ENST00000256084.8:c.1520C>G MANE Select	ENSP00000256084.7:p.Thr507Arg
ENST00000256084.7:c.1520C>G	ENSP00000256084.7:p.Thr507Arg
ENST00000359874.7:c.1520C>G	ENSP00000352936.3:p.Thr507Arg
ENST00000398454.5:c.1520C>G	ENSP00000381472.1:p.Thr507Arg
ENST00000507988.5:n.1684C>G
ENST00000508733.5:c.1463C>G	ENSP00000421519.1:p.Thr488Arg
NM_001127698.1:c.1520C>G	NP_001121170.1:p.Thr507Arg
NM_001127699.1:c.1520C>G	NP_001121171.1:p.Thr507Arg
NM_006846.3:c.1520C>G , LRG_110t1:c.1520C>G	NP_006837.2:p.Thr507Arg
XM_011537550.1:c.1463C>G	XP_011535852.1:p.Thr488Arg
XM_011537551.1:c.1436C>G	XP_011535853.1:p.Thr479Arg
XM_011537551.2:c.1436C>G	XP_011535853.1:p.Thr479Arg
NM_001127698.2:c.1520C>G	NP_001121170.1:p.Thr507Arg
NM_001127699.2:c.1520C>G	NP_001121171.1:p.Thr507Arg
NM_006846.4:c.1520C>G MANE Select	NP_006837.2:p.Thr507Arg