Canonical Allele Identifier: CA357241282

Gene: ALB

Linked Data

• gnomAD v4: 4-73415106-A-T
• MyVariant Identifiers: chr4:g.74280823A>T (hg19) ; chr4:g.73415106A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415106A>T , CM000666.2:g.73415106A>T	GRCh38
NC_000004.11:g.74280823A>T , CM000666.1:g.74280823A>T	GRCh37
NC_000004.10:g.74499687A>T	NCBI36
NG_009291.1:g.15852A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1130A>T MANE Select	ENSP00000295897.4:p.Tyr377Phe
ENST00000295897.8:c.1130A>T	ENSP00000295897.4:p.Tyr377Phe
ENST00000401494.7:c.785A>T	ENSP00000384695.3:p.Tyr262Phe
ENST00000415165.6:c.554A>T	ENSP00000401820.2:p.Tyr185Phe
ENST00000476441.6:c.*409A>T	ENSP00000423727.1:n.*409A>T
ENST00000484992.1:n.450A>T
ENST00000503124.5:c.680A>T	ENSP00000421027.1:p.Tyr227Phe
ENST00000504043.1:n.133A>T
ENST00000505649.5:n.816A>T
ENST00000509063.5:c.1130A>T	ENSP00000422784.1:p.Tyr377Phe
ENST00000511370.1:c.663A>T
ENST00000621085.4:c.491A>T	ENSP00000483421.1:p.Tyr164Phe
ENST00000621628.4:c.491A>T	ENSP00000480485.1:p.Tyr164Phe
NM_000477.5:c.1130A>T	NP_000468.1:p.Tyr377Phe
NM_000477.6:c.1130A>T	NP_000468.1:p.Tyr377Phe
NM_000477.7:c.1130A>T MANE Select	NP_000468.1:p.Tyr377Phe