Canonical Allele Identifier: CA357245267

Gene: ALB

Linked Data

• gnomAD v4: 4-73418281-C-T
• MyVariant Identifiers: chr4:g.74283998C>T (hg19) ; chr4:g.73418281C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418281C>T , CM000666.2:g.73418281C>T	GRCh38
NC_000004.11:g.74283998C>T , CM000666.1:g.74283998C>T	GRCh37
NC_000004.10:g.74502862C>T	NCBI36
NG_009291.1:g.19027C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1622C>T MANE Select	ENSP00000295897.4:p.Ser541Phe
ENST00000295897.8:c.1622C>T	ENSP00000295897.4:p.Ser541Phe
ENST00000401494.7:c.1277C>T	ENSP00000384695.3:p.Ser426Phe
ENST00000415165.6:c.1046C>T	ENSP00000401820.2:p.Ser349Phe
ENST00000476441.6:c.*901C>T	ENSP00000423727.1:n.*901C>T
ENST00000486939.1:n.276C>T
ENST00000503124.5:c.1172C>T	ENSP00000421027.1:p.Ser391Phe
ENST00000505649.5:n.1169C>T
ENST00000509063.5:c.1622C>T	ENSP00000422784.1:p.Ser541Phe
ENST00000511370.1:c.1155C>T
ENST00000621085.4:c.983C>T	ENSP00000483421.1:p.Ser328Phe
ENST00000621628.4:c.983C>T	ENSP00000480485.1:p.Ser328Phe
NM_000477.5:c.1622C>T	NP_000468.1:p.Ser541Phe
NM_000477.6:c.1622C>T	NP_000468.1:p.Ser541Phe
NM_000477.7:c.1622C>T MANE Select	NP_000468.1:p.Ser541Phe