Canonical Allele Identifier: CA3495216

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148088549G>A , CM000667.2:g.148088549G>A	GRCh38
NC_000005.9:g.147468112G>A , CM000667.1:g.147468112G>A	GRCh37
NC_000005.8:g.147448305G>A	NCBI36
NG_009633.1:g.29578G>A , LRG_110:g.29578G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006846.4:c.418G>A MANE Select	NP_006837.2:p.Gly140Arg
ENST00000256084.8:c.418G>A MANE Select	ENSP00000256084.7:p.Gly140Arg
NM_001127698.1:c.418G>A	NP_001121170.1:p.Gly140Arg
NM_001127698.2:c.418G>A	NP_001121170.1:p.Gly140Arg
NM_001127699.1:c.418G>A	NP_001121171.1:p.Gly140Arg
NM_001127699.2:c.418G>A	NP_001121171.1:p.Gly140Arg
NM_006846.3:c.418G>A , LRG_110t1:c.418G>A	NP_006837.2:p.Gly140Arg
ENST00000256084.7:c.418G>A	ENSP00000256084.7:p.Gly140Arg
ENST00000359874.7:c.418G>A	ENSP00000352936.3:p.Gly140Arg
ENST00000398454.5:c.418G>A	ENSP00000381472.1:p.Gly140Arg
ENST00000476697.7:c.418G>A	ENSP00000427943.1:p.Gly140Arg
ENST00000507988.5:n.582G>A
ENST00000508733.5:c.361G>A	ENSP00000421519.1:p.Gly121Arg
ENST00000698105.1:n.288G>A
XM_011537550.1:c.361G>A	XP_011535852.1:p.Gly121Arg
XM_011537551.1:c.334G>A	XP_011535853.1:p.Gly112Arg
XM_011537551.2:c.334G>A	XP_011535853.1:p.Gly112Arg