Canonical Allele Identifier: CA357241088

Gene: ALB

Linked Data

• gnomAD v4: 4-73415051-G-T
• MyVariant Identifiers: chr4:g.74280768G>T (hg19) ; chr4:g.73415051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415051G>T , CM000666.2:g.73415051G>T	GRCh38
NC_000004.11:g.74280768G>T , CM000666.1:g.74280768G>T	GRCh37
NC_000004.10:g.74499632G>T	NCBI36
NG_009291.1:g.15797G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1075G>T MANE Select	ENSP00000295897.4:p.Ala359Ser
ENST00000295897.8:c.1075G>T	ENSP00000295897.4:p.Ala359Ser
ENST00000401494.7:c.730G>T	ENSP00000384695.3:p.Ala244Ser
ENST00000415165.6:c.499G>T	ENSP00000401820.2:p.Ala167Ser
ENST00000476441.6:c.*354G>T	ENSP00000423727.1:n.*354G>T
ENST00000484992.1:n.395G>T
ENST00000503124.5:c.625G>T	ENSP00000421027.1:p.Ala209Ser
ENST00000504043.1:n.78G>T
ENST00000505649.5:n.761G>T
ENST00000509063.5:c.1075G>T	ENSP00000422784.1:p.Ala359Ser
ENST00000511370.1:c.608G>T
ENST00000621085.4:c.491-55G>T	ENSP00000483421.1:n.491-55G>T
ENST00000621628.4:c.487-51G>T	ENSP00000480485.1:n.487-51G>T
NM_000477.5:c.1075G>T	NP_000468.1:p.Ala359Ser
NM_000477.6:c.1075G>T	NP_000468.1:p.Ala359Ser
NM_000477.7:c.1075G>T MANE Select	NP_000468.1:p.Ala359Ser