Canonical Allele Identifier: CA357245018

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283965C>T (hg19) ; chr4:g.73418248C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418248C>T , CM000666.2:g.73418248C>T	GRCh38
NC_000004.11:g.74283965C>T , CM000666.1:g.74283965C>T	GRCh37
NC_000004.10:g.74502829C>T	NCBI36
NG_009291.1:g.18994C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1589C>T MANE Select	ENSP00000295897.4:p.Thr530Ile
ENST00000295897.8:c.1589C>T	ENSP00000295897.4:p.Thr530Ile
ENST00000401494.7:c.1244C>T	ENSP00000384695.3:p.Thr415Ile
ENST00000415165.6:c.1013C>T	ENSP00000401820.2:p.Thr338Ile
ENST00000476441.6:c.*868C>T	ENSP00000423727.1:n.*868C>T
ENST00000486939.1:n.243C>T
ENST00000503124.5:c.1139C>T	ENSP00000421027.1:p.Thr380Ile
ENST00000505649.5:n.1136C>T
ENST00000509063.5:c.1589C>T	ENSP00000422784.1:p.Thr530Ile
ENST00000511370.1:c.1122C>T
ENST00000621085.4:c.950C>T	ENSP00000483421.1:p.Thr317Ile
ENST00000621628.4:c.950C>T	ENSP00000480485.1:p.Thr317Ile
NM_000477.5:c.1589C>T	NP_000468.1:p.Thr530Ile
NM_000477.6:c.1589C>T	NP_000468.1:p.Thr530Ile
NM_000477.7:c.1589C>T MANE Select	NP_000468.1:p.Thr530Ile