Canonical Allele Identifier: CA381554516

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258291G>T (hg19) ; chr11:g.67490820G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490820G>T , CM000673.2:g.67490820G>T	GRCh38
NC_000011.9:g.67258291G>T , CM000673.1:g.67258291G>T	GRCh37
NC_000011.8:g.67014867G>T	NCBI36
NG_008969.1:g.12787G>T , LRG_460:g.12787G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1127G>T
ENST00000528641.7:c.631G>T	ENSP00000434982.3:p.Ala211Ser
ENST00000529797.2:n.1662G>T
ENST00000682324.1:c.469-177G>T	ENSP00000508017.1:n.469-177G>T
ENST00000682659.1:c.451G>T	ENSP00000507351.1:p.Ala151Ser
ENST00000682699.1:c.820G>T	ENSP00000507935.1:p.Ala274Ser
ENST00000683237.1:c.812G>T	ENSP00000507343.1:p.Gly271Val
ENST00000683856.1:c.643G>T	ENSP00000507979.1:p.Ala215Ser
ENST00000684006.1:c.809G>T	ENSP00000507269.1:p.Gly270Val
ENST00000684657.1:c.640G>T	ENSP00000507961.1:p.Ala214Ser
ENST00000279146.8:c.820G>T MANE Select	ENSP00000279146.3:p.Ala274Ser
ENST00000279146.7:c.820G>T	ENSP00000279146.3:p.Ala274Ser
ENST00000528641.6:c.631G>T	ENSP00000434982.2:p.Ala211Ser
NM_001302959.1:c.643G>T	NP_001289888.1:p.Ala215Ser
NM_001302960.1:c.812G>T	NP_001289889.1:p.Gly271Val
NM_003977.3:c.820G>T	NP_003968.3:p.Ala274Ser
XM_024448761.1:c.820G>T	XP_024304529.1:p.Ala274Ser
NM_003977.4:c.820G>T MANE Select	NP_003968.3:p.Ala274Ser
NM_001302960.2:c.812G>T	NP_001289889.1:p.Gly271Val
NM_001302959.2:c.643G>T	NP_001289888.1:p.Ala215Ser