Canonical Allele Identifier: CA4834075

Gene: AZIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102839822G>A , CM000670.2:g.102839822G>A	GRCh38
NC_000008.10:g.103852050G>A , CM000670.1:g.103852050G>A	GRCh37
NC_000008.9:g.103921226G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_148174.4:c.104C>T MANE Select	NP_680479.1:p.Thr35Ile
ENST00000337198.10:c.104C>T MANE Select	ENSP00000337180.5:p.Thr35Ile
NM_001301668.1:c.104C>T	NP_001288597.1:p.Thr35Ile
NM_001301668.2:c.104C>T	NP_001288597.1:p.Thr35Ile
NM_001301668.3:c.104C>T	NP_001288597.1:p.Thr35Ile
NM_001363010.1:c.104C>T	NP_001349939.1:p.Thr35Ile
NM_001363011.1:c.104C>T	NP_001349940.1:p.Thr35Ile
NM_001363012.1:c.104C>T	NP_001349941.1:p.Thr35Ile
NM_001363013.1:c.-549C>T	NP_001349942.1:n.-549C>T
NM_001363014.1:c.-549C>T	NP_001349943.1:n.-549C>T
NM_001363024.1:c.104C>T	NP_001349953.1:p.Thr35Ile
NM_001363083.1:c.104C>T	NP_001350012.1:p.Thr35Ile
NM_015878.5:c.104C>T	NP_056962.2:p.Thr35Ile
NM_148174.3:c.104C>T	NP_680479.1:p.Thr35Ile
ENST00000337198.9:c.104C>T	ENSP00000337180.5:p.Thr35Ile
ENST00000347770.8:c.104C>T	ENSP00000321507.4:p.Thr35Ile
ENST00000520402.5:c.104C>T	ENSP00000429449.1:p.Thr35Ile
ENST00000521536.6:c.103-906C>T	ENSP00000475919.1:n.103-906C>T
ENST00000522311.1:n.231C>T
ENST00000681985.1:c.104C>T	ENSP00000506898.1:p.Thr35Ile
ENST00000682014.1:c.104C>T	ENSP00000507940.1:p.Thr35Ile
ENST00000682725.1:c.104C>T	ENSP00000507451.1:p.Thr35Ile
ENST00000682969.1:c.104C>T	ENSP00000507850.1:p.Thr35Ile
ENST00000683787.1:c.104C>T	ENSP00000508352.1:p.Thr35Ile
ENST00000683965.1:c.104C>T	ENSP00000507890.1:p.Thr35Ile
ENST00000684459.1:c.104C>T	ENSP00000507099.1:p.Thr35Ile
ENST00000684566.1:c.104C>T	ENSP00000506895.1:p.Thr35Ile
ENST00000684721.1:c.104C>T	ENSP00000507711.1:p.Thr35Ile
XM_005250969.1:c.104C>T	XP_005251026.1:p.Thr35Ile
XM_011517126.1:c.104C>T	XP_011515428.1:p.Thr35Ile
XM_011517127.1:c.104C>T	XP_011515429.1:p.Thr35Ile
XM_011517128.1:c.-549C>T	XP_011515430.1:n.-549C>T
XM_017013566.2:c.-549C>T	XP_016869055.1:n.-549C>T