Canonical Allele Identifier: CA308442029

Gene: CEACAM21

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41559909G>A , CM000681.2:g.41559909G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407170.6:c.-778-4773G>A	ENSP00000384380.1:n.-778-4773G>A
ENST00000618577.4:n.36-4773G>A
NM_001288773.2:c.-778-4773G>A	NP_001275702.2:n.-778-4773G>A
XM_011527445.1:c.-779+3824G>A	XP_011525747.1:n.-779+3824G>A
XM_011527446.1:c.-779+3824G>A	XP_011525748.1:n.-779+3824G>A
XM_011527447.1:c.-817+3824G>A	XP_011525749.1:n.-817+3824G>A
XM_011527448.1:c.-779+3824G>A	XP_011525750.1:n.-779+3824G>A
XM_011527449.1:c.-859+3824G>A	XP_011525751.1:n.-859+3824G>A
XM_011527450.1:c.-816-4735G>A	XP_011525752.1:n.-816-4735G>A
XM_011527452.1:c.-778-4773G>A	XP_011525754.1:n.-778-4773G>A
XM_011527454.1:c.-778-4773G>A	XP_011525756.1:n.-778-4773G>A
XM_011527455.1:c.-778-4773G>A	XP_011525757.1:n.-778-4773G>A
XM_011527459.1:c.-779+3824G>A	XP_011525761.1:n.-779+3824G>A
XM_017027433.1:c.-892-4773G>A	XP_016882922.1:n.-892-4773G>A
XM_017027434.2:c.-779+3824G>A	XP_016882923.1:n.-779+3824G>A
XM_017027435.2:c.-779+3824G>A	XP_016882924.1:n.-779+3824G>A
XM_017027436.1:c.-772+3824G>A	XP_016882925.1:n.-772+3824G>A
XM_024451755.1:c.-779+3824G>A	XP_024307523.1:n.-779+3824G>A
XM_024451756.1:c.-779+3824G>A	XP_024307524.1:n.-779+3824G>A
XM_024451757.1:c.-779+3824G>A	XP_024307525.1:n.-779+3824G>A
XM_024451758.1:c.-779+3824G>A	XP_024307526.1:n.-779+3824G>A
XM_024451759.1:c.-779+3824G>A	XP_024307527.1:n.-779+3824G>A
XM_024451760.1:c.-779+3824G>A	XP_024307528.1:n.-779+3824G>A
XM_024451761.1:c.-779+3824G>A	XP_024307529.1:n.-779+3824G>A
XM_024451762.1:c.-859+3824G>A	XP_024307530.1:n.-859+3824G>A
XM_024451763.1:c.-923+3824G>A	XP_024307531.1:n.-923+3824G>A
XM_024451764.1:c.-779+3824G>A	XP_024307532.1:n.-779+3824G>A
XM_024451765.1:c.-817+3824G>A	XP_024307533.1:n.-817+3824G>A
XM_024451766.1:c.-778-4773G>A	XP_024307534.1:n.-778-4773G>A
XM_024451767.1:c.-778-4773G>A	XP_024307535.1:n.-778-4773G>A
NM_001288773.3:c.-778-4773G>A	NP_001275702.2:n.-778-4773G>A