Canonical Allele Identifier: CA357247255

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286005T>C (hg19) ; chr4:g.73420288T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420288T>C , CM000666.2:g.73420288T>C	GRCh38
NC_000004.11:g.74286005T>C , CM000666.1:g.74286005T>C	GRCh37
NC_000004.10:g.74504869T>C	NCBI36
NG_009291.1:g.21034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1820T>C MANE Select	ENSP00000295897.4:p.Leu607Ser
ENST00000295897.8:c.1820T>C	ENSP00000295897.4:p.Leu607Ser
ENST00000401494.7:c.1475T>C	ENSP00000384695.3:p.Leu492Ser
ENST00000415165.6:c.1244T>C	ENSP00000401820.2:p.Leu415Ser
ENST00000476441.6:c.*1099T>C	ENSP00000423727.1:n.*1099T>C
ENST00000495173.1:n.128T>C
ENST00000503124.5:c.1370T>C	ENSP00000421027.1:p.Leu457Ser
ENST00000505649.5:n.1367T>C
ENST00000508932.5:n.210T>C
ENST00000509063.5:c.1785+649T>C	ENSP00000422784.1:n.1785+649T>C
ENST00000511370.1:c.1353T>C
ENST00000621085.4:c.1181T>C	ENSP00000483421.1:p.Leu394Ser
ENST00000621628.4:c.1181T>C	ENSP00000480485.1:p.Leu394Ser
NM_000477.5:c.1820T>C	NP_000468.1:p.Leu607Ser
NM_000477.6:c.1820T>C	NP_000468.1:p.Leu607Ser
NM_000477.7:c.1820T>C MANE Select	NP_000468.1:p.Leu607Ser