Canonical Allele Identifier: CA2675859698

Gene: SPINK5

Linked Data

• gnomAD v4: 5-148131236-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131237del , CM000667.2:g.148131237del	GRCh38
NC_000005.9:g.147510800del , CM000667.1:g.147510800del	GRCh37
NC_000005.8:g.147490993del	NCBI36
NG_009633.1:g.72266del , LRG_110:g.72266del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2965-22del MANE Select	ENSP00000256084.7:n.2965-22del
ENST00000256084.7:c.2965-22del	ENSP00000256084.7:n.2965-22del
ENST00000359874.7:c.3055-22del	ENSP00000352936.3:n.3055-22del
NM_001127698.1:c.3055-22del	NP_001121170.1:n.3055-22del
NM_006846.3:c.2965-22del , LRG_110t1:c.2965-22del	NP_006837.2:n.2965-22del
XM_011537550.1:c.2998-22del	XP_011535852.1:n.2998-22del
XM_011537551.1:c.2971-22del	XP_011535853.1:n.2971-22del
XM_011537551.2:c.2971-22del	XP_011535853.1:n.2971-22del
NM_001127698.2:c.3055-22del	NP_001121170.1:n.3055-22del
NM_006846.4:c.2965-22del MANE Select	NP_006837.2:n.2965-22del