Canonical Allele Identifier: CA798290749

Gene: ALB

Linked Data

• dbSNP Id: rs1217777007
• gnomAD v3: 4-73415183-G-GA
• gnomAD v4: 4-73415183-G-GA
• MyVariant Identifiers: chr4:g.74280900_74280901insA (hg19) ; chr4:g.73415183_73415184insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415190dup , CM000666.2:g.73415190dup	GRCh38
NC_000004.11:g.74280907dup , CM000666.1:g.74280907dup	GRCh37
NC_000004.10:g.74499771dup	NCBI36
NG_009291.1:g.15936dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+23dup MANE Select	ENSP00000295897.4:n.1191+23dup
ENST00000295897.8:c.1191+23dup	ENSP00000295897.4:n.1191+23dup
ENST00000401494.7:c.846+23dup	ENSP00000384695.3:n.846+23dup
ENST00000415165.6:c.615+23dup	ENSP00000401820.2:n.615+23dup
ENST00000476441.6:c.*470+23dup	ENSP00000423727.1:n.*470+23dup
ENST00000484992.1:n.511+23dup
ENST00000503124.5:c.741+23dup	ENSP00000421027.1:n.741+23dup
ENST00000504043.1:n.217dup
ENST00000505649.5:n.877+23dup
ENST00000509063.5:c.1191+23dup	ENSP00000422784.1:n.1191+23dup
ENST00000511370.1:c.724+23dup
ENST00000621085.4:c.552+23dup	ENSP00000483421.1:n.552+23dup
ENST00000621628.4:c.552+23dup	ENSP00000480485.1:n.552+23dup
NM_000477.5:c.1191+23dup	NP_000468.1:n.1191+23dup
NM_000477.6:c.1191+23dup	NP_000468.1:n.1191+23dup
NM_000477.7:c.1191+23dup MANE Select	NP_000468.1:n.1191+23dup