Canonical Allele Identifier: CA446938279

Gene: SPINK5

Linked Data

• gnomAD v4: 5-148131294-C-G
• MyVariant Identifiers: chr5:g.147510857C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131294C>G , CM000667.2:g.148131294C>G	GRCh38
NC_000005.9:g.147510857C>G , CM000667.1:g.147510857C>G	GRCh37
NC_000005.8:g.147491050C>G	NCBI36
NG_009633.1:g.72323C>G , LRG_110:g.72323C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.3000C>G MANE Select	ENSP00000256084.7:p.Pro1000=
ENST00000256084.7:c.3000C>G	ENSP00000256084.7:p.Pro1000=
ENST00000359874.7:c.3090C>G	ENSP00000352936.3:p.Pro1030=
NM_001127698.1:c.3090C>G	NP_001121170.1:p.Pro1030=
NM_006846.3:c.3000C>G , LRG_110t1:c.3000C>G	NP_006837.2:p.Pro1000=
XM_011537550.1:c.3033C>G	XP_011535852.1:p.Pro1011=
XM_011537551.1:c.3006C>G	XP_011535853.1:p.Pro1002=
XM_011537551.2:c.3006C>G	XP_011535853.1:p.Pro1002=
NM_001127698.2:c.3090C>G	NP_001121170.1:p.Pro1030=
NM_006846.4:c.3000C>G MANE Select	NP_006837.2:p.Pro1000=