Canonical Allele Identifier: CA439801094

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285994T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420277T>C , CM000666.2:g.73420277T>C	GRCh38
NC_000004.11:g.74285994T>C , CM000666.1:g.74285994T>C	GRCh37
NC_000004.10:g.74504858T>C	NCBI36
NG_009291.1:g.21023T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1809T>C MANE Select	ENSP00000295897.4:p.Ser603=
ENST00000295897.8:c.1809T>C	ENSP00000295897.4:p.Ser603=
ENST00000401494.7:c.1464T>C	ENSP00000384695.3:p.Ser488=
ENST00000415165.6:c.1233T>C	ENSP00000401820.2:p.Ser411=
ENST00000476441.6:c.*1088T>C	ENSP00000423727.1:n.*1088T>C
ENST00000495173.1:n.117T>C
ENST00000503124.5:c.1359T>C	ENSP00000421027.1:p.Ser453=
ENST00000505649.5:n.1356T>C
ENST00000508932.5:n.199T>C
ENST00000509063.5:c.1785+638T>C	ENSP00000422784.1:n.1785+638T>C
ENST00000511370.1:c.1342T>C
ENST00000621085.4:c.1170T>C	ENSP00000483421.1:p.Ser390=
ENST00000621628.4:c.1170T>C	ENSP00000480485.1:p.Ser390=
NM_000477.5:c.1809T>C	NP_000468.1:p.Ser603=
NM_000477.6:c.1809T>C	NP_000468.1:p.Ser603=
NM_000477.7:c.1809T>C MANE Select	NP_000468.1:p.Ser603=