Canonical Allele Identifier: CA361636927

Gene: SPINK5

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148101392A>T , CM000667.2:g.148101392A>T	GRCh38
NC_000005.9:g.147480955A>T , CM000667.1:g.147480955A>T	GRCh37
NC_000005.8:g.147461148A>T	NCBI36
NG_009633.1:g.42421A>T , LRG_110:g.42421A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.867A>T
ENST00000256084.8:c.1258A>T MANE Select	ENSP00000256084.7:p.Lys420Ter
ENST00000256084.7:c.1258A>T	ENSP00000256084.7:p.Lys420Ter
ENST00000359874.7:c.1258A>T	ENSP00000352936.3:p.Lys420Ter
ENST00000398454.5:c.1258A>T	ENSP00000381472.1:p.Lys420Ter
ENST00000476608.1:n.774A>T
ENST00000507988.5:n.1422A>T
ENST00000508733.5:c.1201A>T	ENSP00000421519.1:p.Lys401Ter
NM_001127698.1:c.1258A>T	NP_001121170.1:p.Lys420Ter
NM_001127699.1:c.1258A>T	NP_001121171.1:p.Lys420Ter
NM_006846.3:c.1258A>T , LRG_110t1:c.1258A>T	NP_006837.2:p.Lys420Ter
XM_011537550.1:c.1201A>T	XP_011535852.1:p.Lys401Ter
XM_011537551.1:c.1174A>T	XP_011535853.1:p.Lys392Ter
XM_011537551.2:c.1174A>T	XP_011535853.1:p.Lys392Ter
NM_001127698.2:c.1258A>T	NP_001121170.1:p.Lys420Ter
NM_001127699.2:c.1258A>T	NP_001121171.1:p.Lys420Ter
NM_006846.4:c.1258A>T MANE Select	NP_006837.2:p.Lys420Ter