Canonical Allele Identifier: CA2670966807

Gene: ALB

Linked Data

• gnomAD v4: 4-73420359-A-ATAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420362_73420365dup , CM000666.2:g.73420362_73420365dup	GRCh38
NC_000004.11:g.74286079_74286082dup , CM000666.1:g.74286079_74286082dup	GRCh37
NC_000004.10:g.74504943_74504946dup	NCBI36
NG_009291.1:g.21108_21111dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+41_*23+44dup MANE Select	ENSP00000295897.4:n.*23+41_*23+44dup
ENST00000295897.8:c.*23+41_*23+44dup	ENSP00000295897.4:n.*23+41_*23+44dup
ENST00000401494.7:c.*23+41_*23+44dup	ENSP00000384695.3:n.*23+41_*23+44dup
ENST00000415165.6:c.*23+41_*23+44dup	ENSP00000401820.2:n.*23+41_*23+44dup
ENST00000476441.6:c.*1132+41_*1132+44dup	ENSP00000423727.1:n.*1132+41_*1132+44dup
ENST00000495173.1:n.161+41_161+44dup
ENST00000503124.5:c.*23+41_*23+44dup	ENSP00000421027.1:n.*23+41_*23+44dup
ENST00000505649.5:n.1400+41_1400+44dup
ENST00000508932.5:n.243+41_243+44dup
ENST00000509063.5:c.1785+723_1786-727dup	ENSP00000422784.1:n.1785+723_1786-727dup
ENST00000511370.1:c.1386+41_1386+44dup
ENST00000621085.4:c.*23+41_*23+44dup	ENSP00000483421.1:n.*23+41_*23+44dup
ENST00000621628.4:c.*23+41_*23+44dup	ENSP00000480485.1:n.*23+41_*23+44dup
NM_000477.5:c.*23+41_*23+44dup	NP_000468.1:n.*23+41_*23+44dup
NM_000477.6:c.*23+41_*23+44dup	NP_000468.1:n.*23+41_*23+44dup
NM_000477.7:c.*23+41_*23+44dup MANE Select	NP_000468.1:n.*23+41_*23+44dup