Canonical Allele Identifier: CA1618471071

Gene: HLA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828657_29828658delinsAC , CM000668.2:g.29828657_29828658delinsAC	GRCh38
NC_000006.11:g.29796434_29796435delinsAC , CM000668.1:g.29796434_29796435delinsAC	GRCh37
NC_000006.10:g.29904413_29904414delinsAC	NCBI36
NG_029039.1:g.6679_6680delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.562_563delinsAC
ENST00000360323.11:c.458_459delinsAC MANE Select	ENSP00000353472.6:p.Asp153=
ENST00000360323.10:c.458_459delinsAC	ENSP00000353472.6:p.Asp153=
ENST00000376815.3:c.343+341_343+342delinsAC	ENSP00000366011.3:n.343+341_343+342delinsAC
ENST00000376818.7:c.343+341_343+342delinsAC	ENSP00000366014.3:n.343+341_343+342delinsAC
ENST00000376828.6:c.473_474delinsAC	ENSP00000366024.2:p.Asp158=
ENST00000428701.5:c.458_459delinsAC	ENSP00000412927.1:p.Asp153=
ENST00000478355.5:n.458_459delinsAC
ENST00000478519.5:c.343+341_343+342delinsAC	ENSP00000436375.1:n.343+341_343+342delinsAC
NM_002127.5:c.458_459delinsAC	NP_002118.1:p.Asp153=
NM_001363567.1:c.473_474delinsAC	NP_001350496.1:p.Asp158=
XM_017010817.1:c.343+341_343+342delinsAC	XP_016866306.1:n.343+341_343+342delinsAC
XM_017010818.1:c.343+341_343+342delinsAC	XP_016866307.1:n.343+341_343+342delinsAC
XM_024446420.1:c.458_459delinsAC	XP_024302188.1:p.Asp153=
NM_001363567.2:c.473_474delinsAC	NP_001350496.1:p.Asp158=
NM_001384280.1:c.473_474delinsAC	NP_001371209.1:p.Asp158=
NM_001384290.1:c.458_459delinsAC MANE Select	NP_001371219.1:p.Asp153=
NM_002127.6:c.458_459delinsAC	NP_002118.1:p.Asp153=