Canonical Allele Identifier: CA2670966809

Gene: ALB

Linked Data

• gnomAD v4: 4-73420362-G-GTTATTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420363_73420370dup , CM000666.2:g.73420363_73420370dup	GRCh38
NC_000004.11:g.74286080_74286087dup , CM000666.1:g.74286080_74286087dup	GRCh37
NC_000004.10:g.74504944_74504951dup	NCBI36
NG_009291.1:g.21109_21116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+42_*23+49dup MANE Select	ENSP00000295897.4:n.*23+42_*23+49dup
ENST00000295897.8:c.*23+42_*23+49dup	ENSP00000295897.4:n.*23+42_*23+49dup
ENST00000401494.7:c.*23+42_*23+49dup	ENSP00000384695.3:n.*23+42_*23+49dup
ENST00000415165.6:c.*23+42_*23+49dup	ENSP00000401820.2:n.*23+42_*23+49dup
ENST00000476441.6:c.*1132+42_*1132+49dup	ENSP00000423727.1:n.*1132+42_*1132+49dup
ENST00000495173.1:n.161+42_161+49dup
ENST00000503124.5:c.*23+42_*23+49dup	ENSP00000421027.1:n.*23+42_*23+49dup
ENST00000505649.5:n.1400+42_1400+49dup
ENST00000508932.5:n.243+42_243+49dup
ENST00000509063.5:c.1785+724_1786-722dup	ENSP00000422784.1:n.1785+724_1786-722dup
ENST00000511370.1:c.1386+42_1386+49dup
ENST00000621085.4:c.*23+42_*23+49dup	ENSP00000483421.1:n.*23+42_*23+49dup
ENST00000621628.4:c.*23+42_*23+49dup	ENSP00000480485.1:n.*23+42_*23+49dup
NM_000477.5:c.*23+42_*23+49dup	NP_000468.1:n.*23+42_*23+49dup
NM_000477.6:c.*23+42_*23+49dup	NP_000468.1:n.*23+42_*23+49dup
NM_000477.7:c.*23+42_*23+49dup MANE Select	NP_000468.1:n.*23+42_*23+49dup