Canonical Allele Identifier: CA439798709

Gene: ALB

Linked Data

• gnomAD v4: 4-73406668-A-C
• MyVariant Identifiers: chr4:g.74272385A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406668A>C , CM000666.2:g.73406668A>C	GRCh38
NC_000004.11:g.74272385A>C , CM000666.1:g.74272385A>C	GRCh37
NC_000004.10:g.74491249A>C	NCBI36
NG_009291.1:g.7414A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.177A>C MANE Select	ENSP00000295897.4:p.Pro59=
ENST00000295897.8:c.177A>C	ENSP00000295897.4:p.Pro59=
ENST00000401494.7:c.137+1495A>C	ENSP00000384695.3:n.137+1495A>C
ENST00000415165.6:c.137+1495A>C	ENSP00000401820.2:n.137+1495A>C
ENST00000441319.5:c.183A>C	ENSP00000392541.1:p.Pro61=
ENST00000476441.6:c.79+2262A>C	ENSP00000423727.1:n.79+2262A>C
ENST00000503124.5:c.-62A>C	ENSP00000421027.1:n.-62A>C
ENST00000509063.5:c.177A>C	ENSP00000422784.1:p.Pro59=
ENST00000510166.5:n.213A>C
ENST00000514786.1:n.146A>C
ENST00000515133.5:n.218A>C
ENST00000621085.4:c.177A>C	ENSP00000483421.1:p.Pro59=
ENST00000621628.4:c.177A>C	ENSP00000480485.1:p.Pro59=
NM_000477.5:c.177A>C	NP_000468.1:p.Pro59=
NM_000477.6:c.177A>C	NP_000468.1:p.Pro59=
NM_000477.7:c.177A>C MANE Select	NP_000468.1:p.Pro59=