Canonical Allele Identifier: CA1589900498

Gene: SPINK5

Linked Data

• dbSNP Id: rs1754411135
• gnomAD v4: 5-148125659-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148125659T>C , CM000667.2:g.148125659T>C	GRCh38
NC_000005.9:g.147505222T>C , CM000667.1:g.147505222T>C	GRCh37
NC_000005.8:g.147485415T>C	NCBI36
NG_009633.1:g.66688T>C , LRG_110:g.66688T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000256084.8:c.2740-64T>C MANE Select	ENSP00000256084.7:n.2740-64T>C
ENST00000256084.7:c.2740-64T>C	ENSP00000256084.7:n.2740-64T>C
ENST00000359874.7:c.2829+46T>C	ENSP00000352936.3:n.2829+46T>C
NM_001127698.1:c.2829+46T>C	NP_001121170.1:n.2829+46T>C
NM_006846.3:c.2740-64T>C , LRG_110t1:c.2740-64T>C	NP_006837.2:n.2740-64T>C
XM_011537550.1:c.2772+46T>C	XP_011535852.1:n.2772+46T>C
XM_011537551.1:c.2745+46T>C	XP_011535853.1:n.2745+46T>C
XM_011537551.2:c.2745+46T>C	XP_011535853.1:n.2745+46T>C
NM_001127698.2:c.2829+46T>C	NP_001121170.1:n.2829+46T>C
NM_006846.4:c.2740-64T>C MANE Select	NP_006837.2:n.2740-64T>C