Canonical Allele Identifier: CA1881249969

Gene: ASS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130458486_130458487delinsAC , CM000671.2:g.130458486_130458487delinsAC	GRCh38
NC_000009.11:g.133333873_133333874delinsAC , CM000671.1:g.133333873_133333874delinsAC	GRCh37
NC_000009.10:g.132323694_132323695delinsAC	NCBI36
NG_011542.1:g.18780_18781delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000352480.10:c.260_261delinsAC MANE Select	ENSP00000253004.6:p.Tyr87=
ENST00000352480.9:c.260_261delinsAC	ENSP00000253004.6:p.Tyr87=
ENST00000372393.7:c.260_261delinsAC	ENSP00000361469.2:p.Tyr87=
ENST00000372394.5:c.260_261delinsAC	ENSP00000361471.1:p.Tyr87=
ENST00000422569.5:c.260_261delinsAC	ENSP00000394212.1:p.Tyr87=
ENST00000443588.1:c.260_261delinsAC	ENSP00000397785.1:p.Tyr87=
NM_000050.4:c.260_261delinsAC	NP_000041.2:p.Tyr87=
NM_054012.3:c.260_261delinsAC	NP_446464.1:p.Tyr87=
XM_005272200.2:c.260_261delinsAC	XP_005272257.1:p.Tyr87=
XM_011518705.1:c.374_375delinsAC	XP_011517007.1:p.Tyr125=
XM_005272200.3:c.260_261delinsAC	XP_005272257.1:p.Tyr87=
XM_011518705.2:c.374_375delinsAC	XP_011517007.1:p.Tyr125=
XM_017014729.1:c.356_357delinsAC	XP_016870218.1:p.Tyr119=
NM_054012.4:c.260_261delinsAC MANE Select	NP_446464.1:p.Tyr87=