Canonical Allele Identifier: CA14822688

Gene: CASS4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56443204T>C , CM000682.2:g.56443204T>C	GRCh38
NC_000020.10:g.55018260T>C , CM000682.1:g.55018260T>C	GRCh37
NC_000020.9:g.54451667T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679529.1:c.298-2696T>C	ENSP00000505834.1:n.298-2696T>C
ENST00000679887.1:c.460-2696T>C MANE Select	ENSP00000506506.1:n.460-2696T>C
ENST00000360314.7:c.460-2696T>C	ENSP00000353462.3:n.460-2696T>C
ENST00000434344.2:c.460-2696T>C	ENSP00000410027.1:n.460-2696T>C
ENST00000497244.1:n.611-2696T>C
NM_001164114.1:c.298-2696T>C	NP_001157586.1:n.298-2696T>C
NM_001164115.1:c.460-2696T>C	NP_001157587.1:n.460-2696T>C
NM_001164116.1:c.460-2696T>C	NP_001157588.1:n.460-2696T>C
NM_020356.3:c.460-2696T>C	NP_065089.2:n.460-2696T>C
XM_006723831.2:c.298-2696T>C	XP_006723894.1:n.298-2696T>C
XM_006723831.3:c.298-2696T>C	XP_006723894.1:n.298-2696T>C
NM_001164114.2:c.298-2696T>C	NP_001157586.1:n.298-2696T>C
NM_001164115.2:c.460-2696T>C	NP_001157587.1:n.460-2696T>C
NM_001164116.2:c.460-2696T>C	NP_001157588.1:n.460-2696T>C
NM_020356.4:c.460-2696T>C MANE Select	NP_065089.2:n.460-2696T>C