Canonical Allele Identifier: CA357244175

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283830G>T (hg19) ; chr4:g.73418113G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418113G>T , CM000666.2:g.73418113G>T	GRCh38
NC_000004.11:g.74283830G>T , CM000666.1:g.74283830G>T	GRCh37
NC_000004.10:g.74502694G>T	NCBI36
NG_009291.1:g.18859G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1454G>T MANE Select	ENSP00000295897.4:p.Cys485Phe
ENST00000295897.8:c.1454G>T	ENSP00000295897.4:p.Cys485Phe
ENST00000401494.7:c.1109G>T	ENSP00000384695.3:p.Cys370Phe
ENST00000415165.6:c.878G>T	ENSP00000401820.2:p.Cys293Phe
ENST00000476441.6:c.*733G>T	ENSP00000423727.1:n.*733G>T
ENST00000486939.1:n.108G>T
ENST00000503124.5:c.1004G>T	ENSP00000421027.1:p.Cys335Phe
ENST00000505649.5:n.1001G>T
ENST00000509063.5:c.1454G>T	ENSP00000422784.1:p.Cys485Phe
ENST00000511370.1:c.987G>T
ENST00000621085.4:c.815G>T	ENSP00000483421.1:p.Cys272Phe
ENST00000621628.4:c.815G>T	ENSP00000480485.1:p.Cys272Phe
NM_000477.5:c.1454G>T	NP_000468.1:p.Cys485Phe
NM_000477.6:c.1454G>T	NP_000468.1:p.Cys485Phe
NM_000477.7:c.1454G>T MANE Select	NP_000468.1:p.Cys485Phe