Canonical Allele Identifier: CA1589892138

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148106995G= , CM000667.2:g.148106995G=	GRCh38
NC_000005.9:g.147486558G= , CM000667.1:g.147486558G=	GRCh37
NC_000005.8:g.147466751G=	NCBI36
NG_009633.1:g.48024G= , LRG_110:g.48024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1089-42G=
ENST00000256084.8:c.1480-42G= MANE Select	ENSP00000256084.7:n.1480-42G=
ENST00000256084.7:c.1480-42G=	ENSP00000256084.7:n.1480-42G=
ENST00000359874.7:c.1480-42G=	ENSP00000352936.3:n.1480-42G=
ENST00000398454.5:c.1480-42G=	ENSP00000381472.1:n.1480-42G=
ENST00000507988.5:n.1644-42G=
ENST00000508733.5:c.1423-42G=	ENSP00000421519.1:n.1423-42G=
NM_001127698.1:c.1480-42G=	NP_001121170.1:n.1480-42G=
NM_001127699.1:c.1480-42G=	NP_001121171.1:n.1480-42G=
NM_006846.3:c.1480-42G= , LRG_110t1:c.1480-42G=	NP_006837.2:n.1480-42G=
XM_011537550.1:c.1423-42G=	XP_011535852.1:n.1423-42G=
XM_011537551.1:c.1396-42G=	XP_011535853.1:n.1396-42G=
XM_011537551.2:c.1396-42G=	XP_011535853.1:n.1396-42G=
NM_001127698.2:c.1480-42G=	NP_001121170.1:n.1480-42G=
NM_001127699.2:c.1480-42G=	NP_001121171.1:n.1480-42G=
NM_006846.4:c.1480-42G= MANE Select	NP_006837.2:n.1480-42G=