Canonical Allele Identifier: CA357238204

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275147A>T (hg19) ; chr4:g.73409430A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409430A>T , CM000666.2:g.73409430A>T	GRCh38
NC_000004.11:g.74275147A>T , CM000666.1:g.74275147A>T	GRCh37
NC_000004.10:g.74494011A>T	NCBI36
NG_009291.1:g.10176A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.558A>T MANE Select	ENSP00000295897.4:p.Lys186Asn
ENST00000295897.8:c.558A>T	ENSP00000295897.4:p.Lys186Asn
ENST00000401494.7:c.213A>T	ENSP00000384695.3:p.Lys71Asn
ENST00000415165.6:c.138-2566A>T	ENSP00000401820.2:n.138-2566A>T
ENST00000441319.5:c.564A>T	ENSP00000392541.1:p.Lys188Asn
ENST00000476441.6:c.155A>T	ENSP00000423727.1:p.Lys52Met
ENST00000503124.5:c.108A>T	ENSP00000421027.1:p.Lys36Asn
ENST00000505649.5:n.244A>T
ENST00000509063.5:c.558A>T	ENSP00000422784.1:p.Lys186Asn
ENST00000511370.1:c.91A>T
ENST00000514786.1:n.527A>T
ENST00000621085.4:c.490+68A>T	ENSP00000483421.1:n.490+68A>T
ENST00000621628.4:c.486+354A>T	ENSP00000480485.1:n.486+354A>T
NM_000477.5:c.558A>T	NP_000468.1:p.Lys186Asn
NM_000477.6:c.558A>T	NP_000468.1:p.Lys186Asn
NM_000477.7:c.558A>T MANE Select	NP_000468.1:p.Lys186Asn