Canonical Allele Identifier: CA357246132

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285251G>T (hg19) ; chr4:g.73419534G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419534G>T , CM000666.2:g.73419534G>T	GRCh38
NC_000004.11:g.74285251G>T , CM000666.1:g.74285251G>T	GRCh37
NC_000004.10:g.74504115G>T	NCBI36
NG_009291.1:g.20280G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1680G>T MANE Select	ENSP00000295897.4:p.Lys560Asn
ENST00000295897.8:c.1680G>T	ENSP00000295897.4:p.Lys560Asn
ENST00000401494.7:c.1335G>T	ENSP00000384695.3:p.Lys445Asn
ENST00000415165.6:c.1104G>T	ENSP00000401820.2:p.Lys368Asn
ENST00000476441.6:c.*959G>T	ENSP00000423727.1:n.*959G>T
ENST00000486939.1:n.334G>T
ENST00000503124.5:c.1230G>T	ENSP00000421027.1:p.Lys410Asn
ENST00000505649.5:n.1227G>T
ENST00000508932.5:n.175+79G>T
ENST00000509063.5:c.1680G>T	ENSP00000422784.1:p.Lys560Asn
ENST00000511370.1:c.1213G>T
ENST00000621085.4:c.1041G>T	ENSP00000483421.1:p.Lys347Asn
ENST00000621628.4:c.1041G>T	ENSP00000480485.1:p.Lys347Asn
NM_000477.5:c.1680G>T	NP_000468.1:p.Lys560Asn
NM_000477.6:c.1680G>T	NP_000468.1:p.Lys560Asn
NM_000477.7:c.1680G>T MANE Select	NP_000468.1:p.Lys560Asn