Canonical Allele Identifier: CA395329007

Gene: KATNIP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27761412G>C , CM000678.2:g.27761412G>C	GRCh38
NC_000016.9:g.27772733G>C , CM000678.1:g.27772733G>C	GRCh37
NC_000016.8:g.27680234G>C	NCBI36
NG_046731.1:g.216266G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015202.5:c.3632-1G>C MANE Select	NP_056017.4:n.3632-1G>C
ENST00000261588.10:c.3632-1G>C MANE Select	ENSP00000261588.4:n.3632-1G>C
NM_015202.2:c.3632-1G>C	NP_056017.2:n.3632-1G>C
NM_015202.3:c.3632-1G>C	NP_056017.3:n.3632-1G>C
NM_015202.4:c.3632-1G>C	NP_056017.3:n.3632-1G>C
ENST00000261588.8:c.3632-1G>C	ENSP00000261588.4:n.3632-1G>C
ENST00000261588.9:c.3632-1G>C	ENSP00000261588.4:n.3632-1G>C
XM_005255201.2:c.3815-1G>C	XP_005255258.1:n.3815-1G>C
XM_005255201.3:c.3815-1G>C	XP_005255258.1:n.3815-1G>C
XM_005255202.2:c.3761-1G>C	XP_005255259.1:n.3761-1G>C
XM_005255202.3:c.3761-1G>C	XP_005255259.1:n.3761-1G>C
XM_005255203.2:c.3686-1G>C	XP_005255260.1:n.3686-1G>C
XM_005255203.3:c.3686-1G>C	XP_005255260.1:n.3686-1G>C
XM_005255206.2:c.3736-1G>C	XP_005255263.1:n.3736-1G>C
XM_005255206.3:c.3736-1G>C	XP_005255263.1:n.3736-1G>C
XM_005255207.2:c.2510-1G>C	XP_005255264.1:n.2510-1G>C
XM_005255208.2:c.2411-1G>C	XP_005255265.1:n.2411-1G>C
XM_006721025.2:c.3554-1G>C	XP_006721088.1:n.3554-1G>C
XM_006721025.3:c.3554-1G>C	XP_006721088.1:n.3554-1G>C
XM_011545773.1:c.3737-1G>C	XP_011544075.1:n.3737-1G>C
XM_011545773.2:c.3737-1G>C	XP_011544075.1:n.3737-1G>C
XM_011545774.1:c.3737-1G>C	XP_011544076.1:n.3737-1G>C
XM_011545774.2:c.3737-1G>C	XP_011544076.1:n.3737-1G>C
XM_011545775.1:c.3695-1G>C	XP_011544077.1:n.3695-1G>C
XM_011545775.2:c.3695-1G>C	XP_011544077.1:n.3695-1G>C
XM_011545776.1:c.3683-1G>C	XP_011544078.1:n.3683-1G>C
XM_011545776.2:c.3683-1G>C	XP_011544078.1:n.3683-1G>C
XM_011545777.1:c.1736-1G>C	XP_011544079.1:n.1736-1G>C
XM_011545777.2:c.1736-1G>C	XP_011544079.1:n.1736-1G>C
XM_017023085.1:c.3566-1G>C	XP_016878574.1:n.3566-1G>C
XM_017023086.1:c.3554-1G>C	XP_016878575.1:n.3554-1G>C
XM_017023087.1:c.3500-1G>C	XP_016878576.1:n.3500-1G>C
XM_017023088.1:c.2510-1G>C	XP_016878577.1:n.2510-1G>C
XM_024450216.1:c.3629-1G>C	XP_024305984.1:n.3629-1G>C
XM_024450217.1:c.3149-1G>C	XP_024305985.1:n.3149-1G>C