Canonical Allele Identifier: CA357240605

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279192A>G (hg19) ; chr4:g.73413475A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413475A>G , CM000666.2:g.73413475A>G	GRCh38
NC_000004.11:g.74279192A>G , CM000666.1:g.74279192A>G	GRCh37
NC_000004.10:g.74498056A>G	NCBI36
NG_009291.1:g.14221A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.899A>G MANE Select	ENSP00000295897.4:p.Lys300Arg
ENST00000295897.8:c.899A>G	ENSP00000295897.4:p.Lys300Arg
ENST00000401494.7:c.554A>G	ENSP00000384695.3:p.Lys185Arg
ENST00000415165.6:c.323A>G	ENSP00000401820.2:p.Lys108Arg
ENST00000476441.6:c.*178A>G	ENSP00000423727.1:n.*178A>G
ENST00000484992.1:n.219A>G
ENST00000503124.5:c.449A>G	ENSP00000421027.1:p.Lys150Arg
ENST00000505649.5:n.585A>G
ENST00000509063.5:c.899A>G	ENSP00000422784.1:p.Lys300Arg
ENST00000511370.1:c.432A>G
ENST00000621085.4:c.491-1631A>G	ENSP00000483421.1:n.491-1631A>G
ENST00000621628.4:c.487-1627A>G	ENSP00000480485.1:n.487-1627A>G
NM_000477.5:c.899A>G	NP_000468.1:p.Lys300Arg
NM_000477.6:c.899A>G	NP_000468.1:p.Lys300Arg
NM_000477.7:c.899A>G MANE Select	NP_000468.1:p.Lys300Arg