Canonical Allele Identifier: CA361647846

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148123905C>T , CM000667.2:g.148123905C>T	GRCh38
NC_000005.9:g.147503468C>T , CM000667.1:g.147503468C>T	GRCh37
NC_000005.8:g.147483661C>T	NCBI36
NG_009633.1:g.64934C>T , LRG_110:g.64934C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006846.4:c.2611C>T MANE Select	NP_006837.2:p.Arg871Ter
ENST00000256084.8:c.2611C>T MANE Select	ENSP00000256084.7:p.Arg871Ter
NM_001127698.1:c.2611C>T	NP_001121170.1:p.Arg871Ter
NM_001127698.2:c.2611C>T	NP_001121170.1:p.Arg871Ter
NM_001127699.1:c.2611C>T	NP_001121171.1:p.Arg871Ter
NM_001127699.2:c.2611C>T	NP_001121171.1:p.Arg871Ter
NM_006846.3:c.2611C>T , LRG_110t1:c.2611C>T	NP_006837.2:p.Arg871Ter
ENST00000256084.7:c.2611C>T	ENSP00000256084.7:p.Arg871Ter
ENST00000359874.7:c.2611C>T	ENSP00000352936.3:p.Arg871Ter
ENST00000398454.5:c.2611C>T	ENSP00000381472.1:p.Arg871Ter
ENST00000508733.5:c.2554C>T	ENSP00000421519.1:p.Arg852Ter
XM_011537550.1:c.2554C>T	XP_011535852.1:p.Arg852Ter
XM_011537551.1:c.2527C>T	XP_011535853.1:p.Arg843Ter
XM_011537551.2:c.2527C>T	XP_011535853.1:p.Arg843Ter