Canonical Allele Identifier: CA1589902846

Gene: SPINK5

Linked Data

• dbSNP Id: rs1437231045
• gnomAD v4: 5-148131203-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131203C>G , CM000667.2:g.148131203C>G	GRCh38
NC_000005.9:g.147510766C>G , CM000667.1:g.147510766C>G	GRCh37
NC_000005.8:g.147490959C>G	NCBI36
NG_009633.1:g.72232C>G , LRG_110:g.72232C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2965-56C>G MANE Select	ENSP00000256084.7:n.2965-56C>G
ENST00000256084.7:c.2965-56C>G	ENSP00000256084.7:n.2965-56C>G
ENST00000359874.7:c.3055-56C>G	ENSP00000352936.3:n.3055-56C>G
NM_001127698.1:c.3055-56C>G	NP_001121170.1:n.3055-56C>G
NM_006846.3:c.2965-56C>G , LRG_110t1:c.2965-56C>G	NP_006837.2:n.2965-56C>G
XM_011537550.1:c.2998-56C>G	XP_011535852.1:n.2998-56C>G
XM_011537551.1:c.2971-56C>G	XP_011535853.1:n.2971-56C>G
XM_011537551.2:c.2971-56C>G	XP_011535853.1:n.2971-56C>G
NM_001127698.2:c.3055-56C>G	NP_001121170.1:n.3055-56C>G
NM_006846.4:c.2965-56C>G MANE Select	NP_006837.2:n.2965-56C>G