Canonical Allele Identifier: CA439800385

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280878C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415161C>A , CM000666.2:g.73415161C>A	GRCh38
NC_000004.11:g.74280878C>A , CM000666.1:g.74280878C>A	GRCh37
NC_000004.10:g.74499742C>A	NCBI36
NG_009291.1:g.15907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1185C>A MANE Select	ENSP00000295897.4:p.Ala395=
ENST00000295897.8:c.1185C>A	ENSP00000295897.4:p.Ala395=
ENST00000401494.7:c.840C>A	ENSP00000384695.3:p.Ala280=
ENST00000415165.6:c.609C>A	ENSP00000401820.2:p.Ala203=
ENST00000476441.6:c.*464C>A	ENSP00000423727.1:n.*464C>A
ENST00000484992.1:n.505C>A
ENST00000503124.5:c.735C>A	ENSP00000421027.1:p.Ala245=
ENST00000504043.1:n.188C>A
ENST00000505649.5:n.871C>A
ENST00000509063.5:c.1185C>A	ENSP00000422784.1:p.Ala395=
ENST00000511370.1:c.718C>A
ENST00000621085.4:c.546C>A	ENSP00000483421.1:p.Ala182=
ENST00000621628.4:c.546C>A	ENSP00000480485.1:p.Ala182=
NM_000477.5:c.1185C>A	NP_000468.1:p.Ala395=
NM_000477.6:c.1185C>A	NP_000468.1:p.Ala395=
NM_000477.7:c.1185C>A MANE Select	NP_000468.1:p.Ala395=