Canonical Allele Identifier: CA1589902850

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131209_148131210delinsCT , CM000667.2:g.148131209_148131210delinsCT	GRCh38
NC_000005.9:g.147510772_147510773delinsCT , CM000667.1:g.147510772_147510773delinsCT	GRCh37
NC_000005.8:g.147490965_147490966delinsCT	NCBI36
NG_009633.1:g.72238_72239delinsCT , LRG_110:g.72238_72239delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2965-50_2965-49delinsCT MANE Select	ENSP00000256084.7:n.2965-50_2965-49delinsCT
ENST00000256084.7:c.2965-50_2965-49delinsCT	ENSP00000256084.7:n.2965-50_2965-49delinsCT
ENST00000359874.7:c.3055-50_3055-49delinsCT	ENSP00000352936.3:n.3055-50_3055-49delinsCT
NM_001127698.1:c.3055-50_3055-49delinsCT	NP_001121170.1:n.3055-50_3055-49delinsCT
NM_006846.3:c.2965-50_2965-49delinsCT , LRG_110t1:c.2965-50_2965-49delinsCT	NP_006837.2:n.2965-50_2965-49delinsCT
XM_011537550.1:c.2998-50_2998-49delinsCT	XP_011535852.1:n.2998-50_2998-49delinsCT
XM_011537551.1:c.2971-50_2971-49delinsCT	XP_011535853.1:n.2971-50_2971-49delinsCT
XM_011537551.2:c.2971-50_2971-49delinsCT	XP_011535853.1:n.2971-50_2971-49delinsCT
NM_001127698.2:c.3055-50_3055-49delinsCT	NP_001121170.1:n.3055-50_3055-49delinsCT
NM_006846.4:c.2965-50_2965-49delinsCT MANE Select	NP_006837.2:n.2965-50_2965-49delinsCT