Canonical Allele Identifier: CA357241396

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280845C>G (hg19) ; chr4:g.73415128C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415128C>G , CM000666.2:g.73415128C>G	GRCh38
NC_000004.11:g.74280845C>G , CM000666.1:g.74280845C>G	GRCh37
NC_000004.10:g.74499709C>G	NCBI36
NG_009291.1:g.15874C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1152C>G MANE Select	ENSP00000295897.4:p.Cys384Trp
ENST00000295897.8:c.1152C>G	ENSP00000295897.4:p.Cys384Trp
ENST00000401494.7:c.807C>G	ENSP00000384695.3:p.Cys269Trp
ENST00000415165.6:c.576C>G	ENSP00000401820.2:p.Cys192Trp
ENST00000476441.6:c.*431C>G	ENSP00000423727.1:n.*431C>G
ENST00000484992.1:n.472C>G
ENST00000503124.5:c.702C>G	ENSP00000421027.1:p.Cys234Trp
ENST00000504043.1:n.155C>G
ENST00000505649.5:n.838C>G
ENST00000509063.5:c.1152C>G	ENSP00000422784.1:p.Cys384Trp
ENST00000511370.1:c.685C>G
ENST00000621085.4:c.513C>G	ENSP00000483421.1:p.Cys171Trp
ENST00000621628.4:c.513C>G	ENSP00000480485.1:p.Cys171Trp
NM_000477.5:c.1152C>G	NP_000468.1:p.Cys384Trp
NM_000477.6:c.1152C>G	NP_000468.1:p.Cys384Trp
NM_000477.7:c.1152C>G MANE Select	NP_000468.1:p.Cys384Trp