Canonical Allele Identifier: CA1139996651

Gene: CHIA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111314586G= , CM000663.2:g.111314586G=	GRCh38
NC_000001.10:g.111857208G= , CM000663.1:g.111857208G=	GRCh37
NC_000001.9:g.111658731G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369740.6:c.304G= MANE Select	ENSP00000358755.1:p.Gly102=
ENST00000343320.10:c.304G=	ENSP00000341828.6:p.Gly102=
ENST00000352594.10:c.-21G=	ENSP00000271312.8:n.-21G=
ENST00000353665.10:c.-153G=	ENSP00000338970.7:n.-153G=
ENST00000369740.5:c.304G=	ENSP00000358755.1:p.Gly102=
ENST00000422815.5:c.136G=	ENSP00000387671.1:p.Gly46=
ENST00000430615.1:c.-21G=	ENSP00000391132.1:n.-21G=
ENST00000451398.6:c.-14G=	ENSP00000390476.2:n.-14G=
ENST00000477918.6:n.109G=
ENST00000483391.5:c.-14G=	ENSP00000436946.1:n.-14G=
ENST00000489524.5:c.-14G=	ENSP00000433309.1:n.-14G=
NM_001040623.2:c.-14G=	NP_001035713.1:n.-14G=
NM_001258001.1:c.-21G=	NP_001244930.1:n.-21G=
NM_001258002.1:c.-14G=	NP_001244931.1:n.-14G=
NM_001258003.1:c.-21G=	NP_001244932.1:n.-21G=
NM_001258004.1:c.-319G=	NP_001244933.1:n.-319G=
NM_001258005.1:c.-153G=	NP_001244934.1:n.-153G=
NM_021797.3:c.-21G=	NP_068569.2:n.-21G=
NM_201653.3:c.304G=	NP_970615.2:p.Gly102=
XM_006710577.2:c.-14G=	XP_006710640.1:n.-14G=
XM_006710577.3:c.-14G=	XP_006710640.1:n.-14G=
XM_017001048.1:c.-21G=	XP_016856537.1:n.-21G=
NM_201653.4:c.304G= MANE Select	NP_970615.2:p.Gly102=
NM_001040623.3:c.-14G=	NP_001035713.1:n.-14G=
NM_001258001.2:c.-21G=	NP_001244930.1:n.-21G=
NM_001258002.2:c.-14G=	NP_001244931.1:n.-14G=
NM_001258003.2:c.-21G=	NP_001244932.1:n.-21G=
NM_001258004.2:c.-319G=	NP_001244933.1:n.-319G=
NM_001258005.2:c.-153G=	NP_001244934.1:n.-153G=
NM_021797.4:c.-21G=	NP_068569.2:n.-21G=