Canonical Allele Identifier: CA99698115

Gene: ALB

Linked Data

• dbSNP Id: rs890837574
• gnomAD v2: 4-74271965-G-GAA
• gnomAD v3: 4-73406248-G-GAA
• gnomAD v4: 4-73406248-G-GAA
• MyVariant Identifiers: chr4:g.74271965_74271966insAA (hg19) ; chr4:g.73406248_73406249insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406249_73406250insAA , CM000666.2:g.73406249_73406250insAA	GRCh38
NC_000004.11:g.74271966_74271967insAA , CM000666.1:g.74271966_74271967insAA	GRCh37
NC_000004.10:g.74490830_74490831insAA	NCBI36
NG_009291.1:g.6995_6996insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-380_138-379insAA MANE Select	ENSP00000295897.4:n.138-380_138-379insAA
ENST00000295897.8:c.138-380_138-379insAA	ENSP00000295897.4:n.138-380_138-379insAA
ENST00000401494.7:c.137+1076_137+1077insAA	ENSP00000384695.3:n.137+1076_137+1077insAA
ENST00000415165.6:c.137+1076_137+1077insAA	ENSP00000401820.2:n.137+1076_137+1077insAA
ENST00000441319.5:c.144-380_144-379insAA	ENSP00000392541.1:n.144-380_144-379insAA
ENST00000476441.6:c.79+1843_79+1844insAA	ENSP00000423727.1:n.79+1843_79+1844insAA
ENST00000503124.5:c.-101-380_-101-379insAA	ENSP00000421027.1:n.-101-380_-101-379insAA
ENST00000509063.5:c.138-380_138-379insAA	ENSP00000422784.1:n.138-380_138-379insAA
ENST00000510166.5:n.174-380_174-379insAA
ENST00000514786.1:n.107-380_107-379insAA
ENST00000515133.5:n.179-380_179-379insAA
ENST00000621085.4:c.138-380_138-379insAA	ENSP00000483421.1:n.138-380_138-379insAA
ENST00000621628.4:c.138-380_138-379insAA	ENSP00000480485.1:n.138-380_138-379insAA
NM_000477.5:c.138-380_138-379insAA	NP_000468.1:n.138-380_138-379insAA
NM_000477.6:c.138-380_138-379insAA	NP_000468.1:n.138-380_138-379insAA
NM_000477.7:c.138-380_138-379insAA MANE Select	NP_000468.1:n.138-380_138-379insAA