Canonical Allele Identifier: CA2694298590

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101400648-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101400648C>A , CM000685.2:g.101400648C>A	GRCh38
NC_000023.10:g.100655636C>A , CM000685.1:g.100655636C>A	GRCh37
NC_000023.9:g.100542292C>A	NCBI36
NG_007119.1:g.12316G>T , LRG_672:g.12316G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*85+18G>T (GLA)	ENSP00000501124.2:n.*85+18G>T
ENST00000674127.2:c.*85+18G>T (GLA)	ENSP00000501044.2:n.*85+18G>T
ENST00000710365.1:c.714+18G>T (GLA)	ENSP00000518234.1:n.714+18G>T
ENST00000218516.4:c.639+18G>T (GLA) MANE Select	ENSP00000218516.4:n.639+18G>T
ENST00000466414.2:n.558+18G>T (GLA)
ENST00000468823.2:n.1574+18G>T (GLA)
ENST00000479445.2:n.1036+18G>T (GLA)
ENST00000480513.6:c.547+984G>T (GLA)	ENSP00000497055.1:n.547+984G>T
ENST00000486121.6:c.684+18G>T (GLA)
ENST00000649178.1:c.762+18G>T (GLA)	ENSP00000498186.1:n.762+18G>T
ENST00000674127.1:c.682+18G>T (GLA)	ENSP00000501044.1:n.682+18G>T
ENST00000674142.1:n.726+18G>T (GLA)
ENST00000674634.2:c.639+18G>T (GLA)	ENSP00000502629.2:n.639+18G>T
ENST00000675592.1:c.639+18G>T (GLA)	ENSP00000502239.1:n.639+18G>T
ENST00000675799.1:c.547+984G>T (GLA)	ENSP00000502661.1:n.547+984G>T
ENST00000675968.1:n.1592G>T (GLA)
ENST00000676156.1:c.603+18G>T (GLA)	ENSP00000501730.1:n.603+18G>T
ENST00000676372.1:c.639+18G>T (GLA)	ENSP00000502805.1:n.639+18G>T
ENST00000218516.3:c.639+18G>T (GLA)	ENSP00000218516.3:n.639+18G>T
ENST00000409170.3:c.300+5191C>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+5191C>A
ENST00000409338.5:c.177+8826C>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+8826C>A
ENST00000468823.1:n.188+18G>T (GLA)
ENST00000480513.5:n.477+984G>T (GLA)
ENST00000486121.5:n.684+18G>T (GLA)
ENST00000493905.6:c.639+18G>T (GLA)	ENSP00000476935.1:n.639+18G>T
NM_000169.2:c.639+18G>T , LRG_672t1:c.639+18G>T (GLA)	NP_000160.1:n.639+18G>T
NM_001199973.1:c.408+5191C>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+5191C>A
NM_001199974.1:c.285+8826C>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+8826C>A
XR_938397.1:n.667+18G>T (GLA)
XR_938397.2:n.688+18G>T (GLA)
NM_001199973.2:c.300+5191C>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+5191C>A
NM_001199974.2:c.177+8826C>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+8826C>A
NM_000169.3:c.639+18G>T (GLA) MANE Select	NP_000160.1:n.639+18G>T
NR_164783.1:n.661+18G>T (GLA)