Canonical Allele Identifier: CA357241392

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280844G>T (hg19) ; chr4:g.73415127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415127G>T , CM000666.2:g.73415127G>T	GRCh38
NC_000004.11:g.74280844G>T , CM000666.1:g.74280844G>T	GRCh37
NC_000004.10:g.74499708G>T	NCBI36
NG_009291.1:g.15873G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1151G>T MANE Select	ENSP00000295897.4:p.Cys384Phe
ENST00000295897.8:c.1151G>T	ENSP00000295897.4:p.Cys384Phe
ENST00000401494.7:c.806G>T	ENSP00000384695.3:p.Cys269Phe
ENST00000415165.6:c.575G>T	ENSP00000401820.2:p.Cys192Phe
ENST00000476441.6:c.*430G>T	ENSP00000423727.1:n.*430G>T
ENST00000484992.1:n.471G>T
ENST00000503124.5:c.701G>T	ENSP00000421027.1:p.Cys234Phe
ENST00000504043.1:n.154G>T
ENST00000505649.5:n.837G>T
ENST00000509063.5:c.1151G>T	ENSP00000422784.1:p.Cys384Phe
ENST00000511370.1:c.684G>T
ENST00000621085.4:c.512G>T	ENSP00000483421.1:p.Cys171Phe
ENST00000621628.4:c.512G>T	ENSP00000480485.1:p.Cys171Phe
NM_000477.5:c.1151G>T	NP_000468.1:p.Cys384Phe
NM_000477.6:c.1151G>T	NP_000468.1:p.Cys384Phe
NM_000477.7:c.1151G>T MANE Select	NP_000468.1:p.Cys384Phe