Canonical Allele Identifier: CA357238073

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275096A>T (hg19) ; chr4:g.73409379A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409379A>T , CM000666.2:g.73409379A>T	GRCh38
NC_000004.11:g.74275096A>T , CM000666.1:g.74275096A>T	GRCh37
NC_000004.10:g.74493960A>T	NCBI36
NG_009291.1:g.10125A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.507A>T MANE Select	ENSP00000295897.4:p.Arg169Ser
ENST00000295897.8:c.507A>T	ENSP00000295897.4:p.Arg169Ser
ENST00000401494.7:c.162A>T	ENSP00000384695.3:p.Arg54Ser
ENST00000415165.6:c.138-2617A>T	ENSP00000401820.2:n.138-2617A>T
ENST00000441319.5:c.513A>T	ENSP00000392541.1:p.Arg171Ser
ENST00000476441.6:c.104A>T	ENSP00000423727.1:p.Asp35Val
ENST00000503124.5:c.57A>T	ENSP00000421027.1:p.Arg19Ser
ENST00000505649.5:n.193A>T
ENST00000509063.5:c.507A>T	ENSP00000422784.1:p.Arg169Ser
ENST00000511370.1:c.40A>T
ENST00000514786.1:n.476A>T
ENST00000621085.4:c.490+17A>T	ENSP00000483421.1:n.490+17A>T
ENST00000621628.4:c.486+303A>T	ENSP00000480485.1:n.486+303A>T
NM_000477.5:c.507A>T	NP_000468.1:p.Arg169Ser
NM_000477.6:c.507A>T	NP_000468.1:p.Arg169Ser
NM_000477.7:c.507A>T MANE Select	NP_000468.1:p.Arg169Ser