Canonical Allele Identifier: CA439800295

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280803G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415086G>T , CM000666.2:g.73415086G>T	GRCh38
NC_000004.11:g.74280803G>T , CM000666.1:g.74280803G>T	GRCh37
NC_000004.10:g.74499667G>T	NCBI36
NG_009291.1:g.15832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1110G>T MANE Select	ENSP00000295897.4:p.Leu370=
ENST00000295897.8:c.1110G>T	ENSP00000295897.4:p.Leu370=
ENST00000401494.7:c.765G>T	ENSP00000384695.3:p.Leu255=
ENST00000415165.6:c.534G>T	ENSP00000401820.2:p.Leu178=
ENST00000476441.6:c.*389G>T	ENSP00000423727.1:n.*389G>T
ENST00000484992.1:n.430G>T
ENST00000503124.5:c.660G>T	ENSP00000421027.1:p.Leu220=
ENST00000504043.1:n.113G>T
ENST00000505649.5:n.796G>T
ENST00000509063.5:c.1110G>T	ENSP00000422784.1:p.Leu370=
ENST00000511370.1:c.643G>T
ENST00000621085.4:c.491-20G>T	ENSP00000483421.1:n.491-20G>T
ENST00000621628.4:c.487-16G>T	ENSP00000480485.1:n.487-16G>T
NM_000477.5:c.1110G>T	NP_000468.1:p.Leu370=
NM_000477.6:c.1110G>T	NP_000468.1:p.Leu370=
NM_000477.7:c.1110G>T MANE Select	NP_000468.1:p.Leu370=