Canonical Allele Identifier: CA805391392

Gene: SPINK5

Linked Data

• dbSNP Id: rs1302180183
• gnomAD v3: 5-148131221-G-A
• gnomAD v4: 5-148131221-G-A
• MyVariant Identifiers: chr5:g.147510784G>A (hg19) ; chr5:g.148131221G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131221G>A , CM000667.2:g.148131221G>A	GRCh38
NC_000005.9:g.147510784G>A , CM000667.1:g.147510784G>A	GRCh37
NC_000005.8:g.147490977G>A	NCBI36
NG_009633.1:g.72250G>A , LRG_110:g.72250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2965-38G>A MANE Select	ENSP00000256084.7:n.2965-38G>A
ENST00000256084.7:c.2965-38G>A	ENSP00000256084.7:n.2965-38G>A
ENST00000359874.7:c.3055-38G>A	ENSP00000352936.3:n.3055-38G>A
NM_001127698.1:c.3055-38G>A	NP_001121170.1:n.3055-38G>A
NM_006846.3:c.2965-38G>A , LRG_110t1:c.2965-38G>A	NP_006837.2:n.2965-38G>A
XM_011537550.1:c.2998-38G>A	XP_011535852.1:n.2998-38G>A
XM_011537551.1:c.2971-38G>A	XP_011535853.1:n.2971-38G>A
XM_011537551.2:c.2971-38G>A	XP_011535853.1:n.2971-38G>A
NM_001127698.2:c.3055-38G>A	NP_001121170.1:n.3055-38G>A
NM_006846.4:c.2965-38G>A MANE Select	NP_006837.2:n.2965-38G>A