Canonical Allele Identifier: CA3496081

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148124769C>T , CM000667.2:g.148124769C>T	GRCh38
NC_000005.9:g.147504332C>T , CM000667.1:g.147504332C>T	GRCh37
NC_000005.8:g.147484525C>T	NCBI36
NG_009633.1:g.65798C>T , LRG_110:g.65798C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006846.4:c.2671C>T MANE Select	NP_006837.2:p.Arg891Ter
ENST00000256084.8:c.2671C>T MANE Select	ENSP00000256084.7:p.Arg891Ter
NM_001127698.1:c.2671C>T	NP_001121170.1:p.Arg891Ter
NM_001127698.2:c.2671C>T	NP_001121170.1:p.Arg891Ter
NM_001127699.1:c.2671C>T	NP_001121171.1:p.Arg891Ter
NM_001127699.2:c.2671C>T	NP_001121171.1:p.Arg891Ter
NM_006846.3:c.2671C>T , LRG_110t1:c.2671C>T	NP_006837.2:p.Arg891Ter
ENST00000256084.7:c.2671C>T	ENSP00000256084.7:p.Arg891Ter
ENST00000359874.7:c.2671C>T	ENSP00000352936.3:p.Arg891Ter
ENST00000398454.5:c.2671C>T	ENSP00000381472.1:p.Arg891Ter
XM_011537550.1:c.2614C>T	XP_011535852.1:p.Arg872Ter
XM_011537551.1:c.2587C>T	XP_011535853.1:p.Arg863Ter
XM_011537551.2:c.2587C>T	XP_011535853.1:p.Arg863Ter