Canonical Allele Identifier: CA3496210

Gene: SPINK5

Linked Data

• ClinVar Variation Id: 260054
• ClinVar RCV Id: RCV000251506 ; RCV000296161 ; RCV001683058 ; RCV003761876
• dbSNP Id: rs58888156
• ExAC: 5:147510812 G / C
• gnomAD v2: 5-147510812-G-C
• gnomAD v3: 5-148131249-G-C
• gnomAD v4: 5-148131249-G-C
• MyVariant Identifiers: chr5:g.147510812G>C (hg19) ; chr5:g.148131249G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131249G>C , CM000667.2:g.148131249G>C	GRCh38
NC_000005.9:g.147510812G>C , CM000667.1:g.147510812G>C	GRCh37
NC_000005.8:g.147491005G>C	NCBI36
NG_009633.1:g.72278G>C , LRG_110:g.72278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2965-10G>C MANE Select	ENSP00000256084.7:n.2965-10G>C
ENST00000256084.7:c.2965-10G>C	ENSP00000256084.7:n.2965-10G>C
ENST00000359874.7:c.3055-10G>C	ENSP00000352936.3:n.3055-10G>C
NM_001127698.1:c.3055-10G>C	NP_001121170.1:n.3055-10G>C
NM_006846.3:c.2965-10G>C , LRG_110t1:c.2965-10G>C	NP_006837.2:n.2965-10G>C
XM_011537550.1:c.2998-10G>C	XP_011535852.1:n.2998-10G>C
XM_011537551.1:c.2971-10G>C	XP_011535853.1:n.2971-10G>C
XM_011537551.2:c.2971-10G>C	XP_011535853.1:n.2971-10G>C
NM_001127698.2:c.3055-10G>C	NP_001121170.1:n.3055-10G>C
NM_006846.4:c.2965-10G>C MANE Select	NP_006837.2:n.2965-10G>C