Canonical Allele Identifier: CA1589897166

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148118470A= , CM000667.2:g.148118470A=	GRCh38
NC_000005.9:g.147498033A= , CM000667.1:g.147498033A=	GRCh37
NC_000005.8:g.147478226A=	NCBI36
NG_009633.1:g.59499A= , LRG_110:g.59499A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2146A= MANE Select	ENSP00000256084.7:p.Asn716=
ENST00000256084.7:c.2146A=	ENSP00000256084.7:p.Asn716=
ENST00000359874.7:c.2146A=	ENSP00000352936.3:p.Asn716=
ENST00000398454.5:c.2146A=	ENSP00000381472.1:p.Asn716=
ENST00000507988.5:n.2310A=
ENST00000508733.5:c.2089A=	ENSP00000421519.1:p.Asn697=
NM_001127698.1:c.2146A=	NP_001121170.1:p.Asn716=
NM_001127699.1:c.2146A=	NP_001121171.1:p.Asn716=
NM_006846.3:c.2146A= , LRG_110t1:c.2146A=	NP_006837.2:p.Asn716=
XM_011537550.1:c.2089A=	XP_011535852.1:p.Asn697=
XM_011537551.1:c.2062A=	XP_011535853.1:p.Asn688=
XM_011537551.2:c.2062A=	XP_011535853.1:p.Asn688=
NM_001127698.2:c.2146A=	NP_001121170.1:p.Asn716=
NM_001127699.2:c.2146A=	NP_001121171.1:p.Asn716=
NM_006846.4:c.2146A= MANE Select	NP_006837.2:p.Asn716=