Canonical Allele Identifier: CA2670966763

Gene: ALB

Linked Data

• gnomAD v4: 4-73420244-TTGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420246_73420249del , CM000666.2:g.73420246_73420249del	GRCh38
NC_000004.11:g.74285963_74285966del , CM000666.1:g.74285963_74285966del	GRCh37
NC_000004.10:g.74504827_74504830del	NCBI36
NG_009291.1:g.20992_20995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-8_1786-5del MANE Select	ENSP00000295897.4:n.1786-8_1786-5del
ENST00000295897.8:c.1786-8_1786-5del	ENSP00000295897.4:n.1786-8_1786-5del
ENST00000401494.7:c.1441-8_1441-5del	ENSP00000384695.3:n.1441-8_1441-5del
ENST00000415165.6:c.1210-8_1210-5del	ENSP00000401820.2:n.1210-8_1210-5del
ENST00000476441.6:c.*1065-8_*1065-5del	ENSP00000423727.1:n.*1065-8_*1065-5del
ENST00000495173.1:n.94-8_94-5del
ENST00000503124.5:c.1336-8_1336-5del	ENSP00000421027.1:n.1336-8_1336-5del
ENST00000505649.5:n.1333-8_1333-5del
ENST00000508932.5:n.176-8_176-5del
ENST00000509063.5:c.1785+607_1785+610del	ENSP00000422784.1:n.1785+607_1785+610del
ENST00000511370.1:c.1319-8_1319-5del
ENST00000621085.4:c.1147-8_1147-5del	ENSP00000483421.1:n.1147-8_1147-5del
ENST00000621628.4:c.1147-8_1147-5del	ENSP00000480485.1:n.1147-8_1147-5del
NM_000477.5:c.1786-8_1786-5del	NP_000468.1:n.1786-8_1786-5del
NM_000477.6:c.1786-8_1786-5del	NP_000468.1:n.1786-8_1786-5del
NM_000477.7:c.1786-8_1786-5del MANE Select	NP_000468.1:n.1786-8_1786-5del