Canonical Allele Identifier: CA357238080

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275098A>T (hg19) ; chr4:g.73409381A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409381A>T , CM000666.2:g.73409381A>T	GRCh38
NC_000004.11:g.74275098A>T , CM000666.1:g.74275098A>T	GRCh37
NC_000004.10:g.74493962A>T	NCBI36
NG_009291.1:g.10127A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.509A>T MANE Select	ENSP00000295897.4:p.His170Leu
ENST00000295897.8:c.509A>T	ENSP00000295897.4:p.His170Leu
ENST00000401494.7:c.164A>T	ENSP00000384695.3:p.His55Leu
ENST00000415165.6:c.138-2615A>T	ENSP00000401820.2:n.138-2615A>T
ENST00000441319.5:c.515A>T	ENSP00000392541.1:p.His172Leu
ENST00000476441.6:c.106A>T	ENSP00000423727.1:p.Ile36Phe
ENST00000503124.5:c.59A>T	ENSP00000421027.1:p.His20Leu
ENST00000505649.5:n.195A>T
ENST00000509063.5:c.509A>T	ENSP00000422784.1:p.His170Leu
ENST00000511370.1:c.42A>T
ENST00000514786.1:n.478A>T
ENST00000621085.4:c.490+19A>T	ENSP00000483421.1:n.490+19A>T
ENST00000621628.4:c.486+305A>T	ENSP00000480485.1:n.486+305A>T
NM_000477.5:c.509A>T	NP_000468.1:p.His170Leu
NM_000477.6:c.509A>T	NP_000468.1:p.His170Leu
NM_000477.7:c.509A>T MANE Select	NP_000468.1:p.His170Leu