Canonical Allele Identifier: CA2706482951

Gene: ALB

Linked Data

• dbSNP Id: rs2149329623

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418247dup , CM000666.2:g.73418247dup	GRCh38
NC_000004.11:g.74283964dup , CM000666.1:g.74283964dup	GRCh37
NC_000004.10:g.74502828dup	NCBI36
NG_009291.1:g.18993dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1588dup MANE Select	ENSP00000295897.4:p.Thr530AsnfsTer13
ENST00000295897.8:c.1588dup	ENSP00000295897.4:p.Thr530AsnfsTer13
ENST00000401494.7:c.1243dup	ENSP00000384695.3:p.Thr415AsnfsTer13
ENST00000415165.6:c.1012dup	ENSP00000401820.2:p.Thr338AsnfsTer13
ENST00000476441.6:c.*867dup	ENSP00000423727.1:n.*867dup
ENST00000486939.1:n.242dup
ENST00000503124.5:c.1138dup	ENSP00000421027.1:p.Thr380AsnfsTer13
ENST00000505649.5:n.1135dup
ENST00000509063.5:c.1588dup	ENSP00000422784.1:p.Thr530AsnfsTer13
ENST00000511370.1:c.1121dup
ENST00000621085.4:c.949dup	ENSP00000483421.1:p.Thr317AsnfsTer13
ENST00000621628.4:c.949dup	ENSP00000480485.1:p.Thr317AsnfsTer13
NM_000477.5:c.1588dup	NP_000468.1:p.Thr530AsnfsTer13
NM_000477.6:c.1588dup	NP_000468.1:p.Thr530AsnfsTer13
NM_000477.7:c.1588dup MANE Select	NP_000468.1:p.Thr530AsnfsTer13